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

rs397507282

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507282(C;G)
Make rs397507282(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336586
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507282
ebirs397507282
HLIrs397507282
Exacrs397507282
Varsomers397507282
Maprs397507282
PheGenIrs397507282
hapmaprs397507282
1000 genomesrs397507282
hgdprs397507282
ensemblrs397507282
gopubmedrs397507282
geneviewrs397507282
scholarrs397507282
googlers397507282
pharmgkbrs397507282
gwascentralrs397507282
openSNPrs397507282
23andMers397507282
23andMe allrs397507282
SNP Nexus

SNPshotrs397507282
SNPdbers397507282
MSV3drs397507282
GWAS Ctlgrs397507282
Max Magnitude0
ClinVar
Risk rs397507282(G,T;G,T)
Alt rs397507282(G,T;G,T)
Reference rs397507282(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32910723C>A; NC_000013.10:g.32910723C>G; NC_000013.10:g.32910723C>T
CLNSRC ClinVar
CLNACC RCV000216087.1, RCV000031358.3, RCV000043959.2, RCV000166823.1,