RGD:153349946 Rat Genome Database

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Variant: RGD:153349946 -  Homo sapiens

RGD ID: 153349946
RS ID: rs562520783
ClinVar ID: CV1693626
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 73,600,361
GRCh38 14 73,133,653
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_224:g.2183A>G
NG_007386.2:g.2183A>G
NC_000014.9:g.73133653A>G
NC_000014.8:g.73600361A>G
 09/01/2019 uncertain significance none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002276382 CLINVAR
dbSNP (RS) rs562520783 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PSEN1 CLINVAR
OMIM 104311 CLINVAR