rs7181375 Rat Genome Database

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Variant: rs7181375 -  Homo sapiens

RGD ID: 150337870
RS ID: rs7181375
ClinVar ID: CV1172686
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 36,871,473
GRCh38 15 36,579,272
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_034055.1:g.4670C>T
NC_000015.10:g.36579272C>T
NC_000015.9:g.36871473C>T
 06/18/2021 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001541888 CLINVAR
dbSNP (RS) rs7181375 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CDIN1 CLINVAR
OMIM 615626 CLINVAR