RGD:150484232 Rat Genome Database

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Variant: RGD:150484232 -  Homo sapiens

RGD ID: 150484232
RS ID: rs2597780
ClinVar ID: CV1245254
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 17,514,160
GRCh38 4 17,512,537
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_008763.1:g.4698G>A
NC_000004.12:g.17512537C>T
NC_000004.11:g.17514160C>T
 07/27/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001653431 CLINVAR
dbSNP (RS) rs2597780 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene QDPR CLINVAR
OMIM 612676 CLINVAR