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rs397507881

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507881(G;T)
Make rs397507881(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32316527
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507881
ebirs397507881
HLIrs397507881
Exacrs397507881
Varsomers397507881
Maprs397507881
PheGenIrs397507881
hapmaprs397507881
1000 genomesrs397507881
hgdprs397507881
ensemblrs397507881
gopubmedrs397507881
geneviewrs397507881
scholarrs397507881
googlers397507881
pharmgkbrs397507881
gwascentralrs397507881
openSNPrs397507881
23andMers397507881
23andMe allrs397507881
SNP Nexus

SNPshotrs397507881
SNPdbers397507881
MSV3drs397507881
GWAS Ctlgrs397507881
Max Magnitude0
ClinVar
Risk rs397507881(T;T)
Alt rs397507881(T;T)
Reference rs397507881(G;G)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32890664G>A; NC_000013.10:g.32890664G>T
CLNSRC
CLNACC RCV000211034.1, RCV000045049.2,