RGD:150464601 Rat Genome Database

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Variant: RGD:150464601 -  Homo sapiens

RGD ID: 150464601
RS ID: rs12037379
ClinVar ID: CV1241331
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 20,959,746
GRCh38 1 20,633,253
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_008164.1:g.4799T>C
NC_000001.11:g.20633253T>C
NC_000001.10:g.20959746T>C
 07/09/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001649842 CLINVAR
dbSNP (RS) rs12037379 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PINK1 CLINVAR
OMIM 608309 CLINVAR