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

rs397508037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508037(C;T)
Make rs397508037(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379905
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508037
ebirs397508037
HLIrs397508037
Exacrs397508037
Varsomers397508037
Maprs397508037
PheGenIrs397508037
hapmaprs397508037
1000 genomesrs397508037
hgdprs397508037
ensemblrs397508037
gopubmedrs397508037
geneviewrs397508037
scholarrs397508037
googlers397508037
pharmgkbrs397508037
gwascentralrs397508037
openSNPrs397508037
23andMers397508037
23andMe allrs397508037
SNP Nexus

SNPshotrs397508037
SNPdbers397508037
MSV3drs397508037
GWAS Ctlgrs397508037
Max Magnitude0
ClinVar
Risk rs397508037(T;T)
Alt rs397508037(T;T)
Reference rs397508037(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32954042C>T
CLNSRC ClinVar
CLNACC RCV000045719.2, RCV000083153.3,