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rs397507638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs397507638(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337103
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507638
dbSNP (classic)rs397507638
ClinGenrs397507638
ebirs397507638
HLIrs397507638
Exacrs397507638
Gnomadrs397507638
Varsomers397507638
LitVarrs397507638
Maprs397507638
PheGenIrs397507638
Biobankrs397507638
1000 genomesrs397507638
hgdprs397507638
ensemblrs397507638
geneviewrs397507638
scholarrs397507638
googlers397507638
pharmgkbrs397507638
gwascentralrs397507638
openSNPrs397507638
23andMers397507638
SNPshotrs397507638
SNPdbers397507638
MSV3drs397507638
GWAS Ctlgrs397507638
Max Magnitude6
ClinVar
Risk rs397507638(A;A)
Alt rs397507638(A;A)
Reference Rs397507638(T;T)
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.32911240T>A
CLNSRC ClinVar
CLNACC RCV000044047.2, RCV000257471.2,