Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507274(A;A)
Make rs397507274(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333183
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507274
ebirs397507274
HLIrs397507274
Exacrs397507274
Varsomers397507274
Maprs397507274
PheGenIrs397507274
hapmaprs397507274
1000 genomesrs397507274
hgdprs397507274
ensemblrs397507274
gopubmedrs397507274
geneviewrs397507274
scholarrs397507274
googlers397507274
pharmgkbrs397507274
gwascentralrs397507274
openSNPrs397507274
23andMers397507274
23andMe allrs397507274
SNP Nexus

SNPshotrs397507274
SNPdbers397507274
MSV3drs397507274
GWAS Ctlgrs397507274
Max Magnitude0
ClinVar
Risk rs397507274(A;A)
Alt rs397507274(A;A)
Reference rs397507274(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations not specified
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations not specified
Reversed 0
HGVS NC_000013.10:g.32907320C>A
CLNSRC ClinVar
CLNACC RCV000031333.3, RCV000215568.1, RCV000220050.1,