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rs397507939

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507939(G;G)
Make rs397507939(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362514
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507939
ebirs397507939
HLIrs397507939
Exacrs397507939
Varsomers397507939
Maprs397507939
PheGenIrs397507939
hapmaprs397507939
1000 genomesrs397507939
hgdprs397507939
ensemblrs397507939
gopubmedrs397507939
geneviewrs397507939
scholarrs397507939
googlers397507939
pharmgkbrs397507939
gwascentralrs397507939
openSNPrs397507939
23andMers397507939
23andMe allrs397507939
SNP Nexus

SNPshotrs397507939
SNPdbers397507939
MSV3drs397507939
GWAS Ctlgrs397507939
Max Magnitude0
ClinVar
Risk rs397507939(G;G)
Alt rs397507939(G;G)
Reference rs397507939(T;T)
Significance Untested
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.32936651T>G
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045323.2, RCV000113827.1,