RGD:243055732 Rat Genome Database

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Variant: RGD:243055732 -  Homo sapiens

RGD ID: 243055732
RS ID: rs754802246
ClinVar ID: CV2416009
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 6,305,829
GRCh38 4 6,304,102
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_011700.1:g.39253C>A
LRG_1417:g.39253C>A
NC_000004.12:g.6304102C>A
NC_000004.11:g.6305829C>A
 benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:12955714   PMID:17603484   PMID:18060660   PMID:20301750   PMID:20738327   PMID:33879153  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003149065 CLINVAR
dbSNP (RS) rs754802246 CLINVAR
MedGen C4551693 CLINVAR
NCBI Gene WFS1 CLINVAR
OMIM 222300 CLINVAR
  606201 CLINVAR