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GENE - TERM ANNOTATION REPORT

96 Annotations Found.

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13531200 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999 PMID:23195492

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624325 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:17347258 PMID:25459968

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13530764 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:21248271 PMID:24097157 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10054613 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11254445 PMID:24168886 PMID:26096185

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12894195 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:23195492 PMID:28492532 PMID:31302675

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624319 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12083760 PMID:17347258 PMID:18554359 PMID:20431604 PMID:22780858 PMID:23762420 PMID:25741868 PMID:26096185 PMID:28186331 PMID:28492532 PMID:29141279 PMID:30182498

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10398068 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:26680202 PMID:28492532 PMID:28735751 PMID:28842445 PMID:29655203

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10396771 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:21248271 PMID:21719429 PMID:23884151 PMID:25741868 PMID:26467025 PMID:27231140 PMID:28492532 PMID:29739726

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10054601 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12566275 PMID:17347258 PMID:18930999 PMID:23195492 PMID:23934111 PMID:24168886 PMID:25741868 PMID:26096185 PMID:26232052 PMID:26467025 PMID:28492532 PMID:29186148

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12836231 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:17576681 PMID:28492532 PMID:9536098

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8640567 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11940708 PMID:17347258 PMID:17537961 PMID:18930999 PMID:24155976 PMID:24502503 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8640578 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12610651 PMID:18414213 PMID:21713554 PMID:22011963 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13828304 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:19339291 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155685887 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12083760

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151232864 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:29601086

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8569744 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:24337656 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624370 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11254445 PMID:12610651 PMID:19200853 PMID:19522081 PMID:23195492 PMID:25741868 PMID:26990884 PMID:28492532 PMID:29358611

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624305 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:14738421 PMID:15277629 PMID:15508916 PMID:16713913 PMID:16713920 PMID:17166794 PMID:17347258 PMID:18930999 PMID:19589774 PMID:20550552 PMID:21248271 PMID:21371021 PMID:21864321 PMID:23195492 PMID:25741868 PMID:26467025 PMID:27781031 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151841664 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11359211 PMID:15880351 PMID:16458823 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155676330 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:24848745

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624398 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11254445 PMID:18021921 PMID:21396429 PMID:22550089 PMID:22780858 PMID:23398611 PMID:24679980 PMID:25741868 PMID:26990884 PMID:28492532 PMID:29358611 PMID:31765958

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13830083 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28202706 PMID:28492532 PMID:28951233

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155745816 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:15087100 PMID:18930999 PMID:19585586 PMID:23195492 PMID:28183995 PMID:29429461

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155739070 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28735751

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8591780 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18414213 PMID:18930999 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10406793 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18414213 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155741079 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:23195492 PMID:28735751

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13830387 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18413471 PMID:26096185

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10396746 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:27029629 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624316 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999 PMID:19522081 PMID:20729507 PMID:25741868 PMID:26990884 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:127262563 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18076640 PMID:19585586 PMID:22151702 PMID:25741868 PMID:25754450 PMID:28492532 PMID:28735751

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10054706 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999 PMID:19782004 PMID:24168886 PMID:26096185 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11632992 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:21248271 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8660589 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18414213 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10054731 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:16199547 PMID:17347258 PMID:18930999 PMID:25741868 PMID:26096185 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10051236 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:20452746 PMID:26467025 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13829635 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:23195492

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10051235 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:20729507 PMID:26467025 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155709313 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8563360 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:10521305 PMID:10742094 PMID:11567038 PMID:12086636 PMID:14702334 PMID:18930999 PMID:20522430 PMID:23195492 PMID:25741868 PMID:28192756 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10396763 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28492532 PMID:29655203 PMID:31765958

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624340 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:17347258 PMID:19359143 PMID:19589774 PMID:25741868 PMID:27864847 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10050412 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11254445 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:9693317 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:26467025 PMID:26699486 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8640560 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11254444 PMID:12610651 PMID:14504318 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8640561 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13476624 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13830386 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:20196795 PMID:26680202 PMID:27781031

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10398039 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25754450 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13830401 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:21248271 PMID:21719429 PMID:23195492 PMID:24136861 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155664498 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:17054684 PMID:29408779 PMID:29745119

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8640544 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11254445 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624371 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11254445 PMID:18930999 PMID:19236456 PMID:19589774 PMID:20879882 PMID:21713554 PMID:25741868 PMID:26467025 PMID:26845707 PMID:26990884 PMID:27236449 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155670904 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12566275 PMID:28012175 PMID:28183995

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13520517 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999 PMID:23884151 PMID:24066114 PMID:24136861 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624364 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:20729507 PMID:21719429 PMID:26990884 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624356 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11254444 PMID:18056581 PMID:18413471 PMID:18930999 PMID:21713554 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8591802 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11359211 PMID:12821740 PMID:14738421 PMID:17347258 PMID:18930999 PMID:19522081 PMID:20879882 PMID:22150645 PMID:22612257 PMID:23195492 PMID:24168886 PMID:25741868 PMID:26096185 PMID:28492532 PMID:29100083

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624420 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999 PMID:19563458 PMID:20452746 PMID:22848613 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13830443 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:20738378 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10054748 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:23195492 PMID:26096185

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:38497891 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25459968 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10396753 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:28492532 PMID:29948376

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:9688397 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12821740 PMID:17054684 PMID:17347258 PMID:18930999 PMID:21906962 PMID:25741868 PMID:26096185 PMID:26467025 PMID:26544041 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:38490325 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:26394714 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12849484 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:21868258 PMID:24472396 PMID:26680202 PMID:28492532 PMID:31009440

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13828966 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:16199547 PMID:17347258 PMID:18930999 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:127288365 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18930999 PMID:25525159 PMID:25741868 PMID:28150151

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10398054 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:23398550 PMID:25741868 PMID:28492532 PMID:29655203 PMID:33391346

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8640563 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:23398550 PMID:25741868 PMID:28492532 PMID:29655203

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10054590 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:16541393 PMID:17054684 PMID:17347258 PMID:18930999 PMID:20431604 PMID:20522430 PMID:24168886 PMID:25741868 PMID:26096185 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10398036 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:17347258 PMID:18930999 PMID:19673951 PMID:21248271 PMID:25741868 PMID:25754450 PMID:26467025 PMID:28488083 PMID:28492532 PMID:31164858 PMID:31864146

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10396776 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:28492532 PMID:28518168 PMID:32461654

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151738451 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28492532 PMID:28735751 PMID:29852413

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624290 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:16713920 PMID:17347258 PMID:19586930 PMID:28150151 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:14724505 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:19350499 PMID:26934580 PMID:28202706 PMID:28492532 PMID:28518218

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:14722973 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28012175 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10396752 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:19522081 PMID:21719429 PMID:25741868 PMID:26990884 PMID:28492532 PMID:31009440

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:150487412 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28202706 PMID:28469861 PMID:28492532 PMID:28664031 PMID:31875159 PMID:32613771 PMID:35074891

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11559679 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12083760 PMID:17347258 PMID:18755274 PMID:18930999 PMID:22092154 PMID:24412860 PMID:25525159 PMID:25741868 PMID:28492532 PMID:29852413 PMID:31755124 PMID:31864146 PMID:33278787 PMID:35074891 PMID:36684540

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624339 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:17347258 PMID:19589774 PMID:25741868 PMID:26633542 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8569743|RGD:8591779|RGD:8692721 (Homo sapiens) & RGD:8569743|RGD:8591779|RGD:8692721 (Homo sapiens) & RGD:8569743|RGD:8591779|RGD:8692721 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens) & RGD:10047879|RGD:10396721|RGD:10396740|RGD:10396749|RGD:10396751|RGD:10396770|RGD:10396781|RGD:11581211|RGD:11581700|RGD:11581868|RGD:11637878|RGD:11638651|RGD:11641297|RGD:11642297|RGD:126749992|RGD:126770004|RGD:126772786|RGD:127245774|RGD:127247472|RGD:127261769|RGD:127278714|RGD:127279927|RGD:12832917|RGD:12833764|RGD:12835582|RGD:12838166|RGD:12843073|RGD:12846914|RGD:13496448|RGD:13521767|RGD:13523889|RGD:13541248|RGD:13620564|RGD:13620580|RGD:13818438|RGD:13828912|RGD:13829127|RGD:13830385|RGD:13830656|RGD:13830757|RGD:14704811|RGD:14743378|RGD:15113680|RGD:15139691|RGD:15146429|RGD:153301633|RGD:155701529|RGD:155743039|RGD:155743347|RGD:155951073|RGD:21067389|RGD:26907728|RGD:26917206|RGD:38471014|RGD:38479288|RGD:8692722 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624317 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:18413471 PMID:18554359 PMID:26096185 PMID:28492532 PMID:34268891

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624395 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12610651 PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens) & RGD:10396724|RGD:10396736|RGD:10396756|RGD:10396759|RGD:10396760|RGD:10403521|RGD:12832961|RGD:12846341|RGD:12905870|RGD:13216334|RGD:13465784|RGD:13479276|RGD:13519726|RGD:13523440|RGD:13620635|RGD:14701318|RGD:14740465|RGD:150410227|RGD:151736081|RGD:152139575|RGD:155700756|RGD:26915295|RGD:8640573|RGD:8640575|RGD:8640579|RGD:8692709|RGD:8692715|RGD:8692716|RGD:8692718|RGD:8692720 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10396738|RGD:12905853|RGD:8640564 (Homo sapiens) & RGD:10396738|RGD:12905853|RGD:8640564 (Homo sapiens) & RGD:10396738|RGD:12905853|RGD:8640564 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:26467025 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10398132 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28492532 PMID:29655203

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8624367 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:12566275 PMID:17576681 PMID:18930999 PMID:19585586 PMID:24502503 PMID:28012175 PMID:28150151 PMID:28492532 PMID:35074891 PMID:9536098

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10767250 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25795284 PMID:28492532 PMID:35571373

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:150414383 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:17347258 PMID:18930999 PMID:25356970 PMID:26795593 PMID:28492532

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens) & RGD:10401589|RGD:11560129|RGD:13517530|RGD:13530503|RGD:13533119|RGD:13828963|RGD:13829351|RGD:13829503|RGD:13830516|RGD:13830787|RGD:155663794|RGD:155669134|RGD:155673516|RGD:155683402|RGD:155683715|RGD:155688106|RGD:155694724|RGD:155704632|RGD:155708924|RGD:155714616|RGD:155721708|RGD:155724291|RGD:155724842|RGD:155724890|RGD:155739128|RGD:155907667|RGD:155914998|RGD:155962199|RGD:155994114|RGD:156046631|RGD:156123489|RGD:329396222|RGD:401743043|RGD:401774022|RGD:401779309|RGD:40887388|RGD:40887968 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10401592|RGD:13532495|RGD:156074509 (Homo sapiens) & RGD:10401592|RGD:13532495|RGD:156074509 (Homo sapiens) & RGD:10401592|RGD:13532495|RGD:156074509 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:25741868

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:155742165 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:28492532 PMID:33895391

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12741938 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:27959697 PMID:28202706 PMID:28492532 PMID:35074891

An association has been curated linking SCN1A and genetic disease in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10047768 (Homo sapiens)
33187 RGD objects have been annotated to genetic disease  (DOID:630)
8 papers in RGD have been used to annotate SCN1A
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
Original References(s): PMID:11940708 PMID:12083760 PMID:16458823 PMID:17347258 PMID:18804930 PMID:18930999 PMID:20522430 PMID:21248271 PMID:22151702 PMID:23195492 PMID:23808377 PMID:25741868 PMID:26096185 PMID:26467025 PMID:26544041 PMID:28079314 PMID:28387369 PMID:28492532 PMID:29100083 PMID:31864146 PMID:32056211 PMID:32090326 PMID:35571373

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