rs72704491 Rat Genome Database

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Variant: rs72704491 -  Homo sapiens

RGD ID: 150500757
RS ID: rs72704491
ClinVar ID: CV1283825
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 36,871,615
GRCh38 15 36,579,414
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_034055.1:g.4812G>A
NC_000015.10:g.36579414G>A
NC_000015.9:g.36871615G>A
 06/18/2021 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001718459 CLINVAR
dbSNP (RS) rs72704491 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CDIN1 CLINVAR
OMIM 615626 CLINVAR