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rs397507796

From SNPedia

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


Make rs397507796(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340020
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507796
dbSNP (old)rs397507796
ClinGenrs397507796
ebirs397507796
HLIrs397507796
Exacrs397507796
Varsomers397507796
Maprs397507796
PheGenIrs397507796
Biobankrs397507796
1000 genomesrs397507796
hgdprs397507796
ensemblrs397507796
gopubmedrs397507796
geneviewrs397507796
scholarrs397507796
googlers397507796
pharmgkbrs397507796
gwascentralrs397507796
openSNPrs397507796
23andMers397507796
23andMe allrs397507796
SNP Nexus

SNPshotrs397507796
SNPdbers397507796
MSV3drs397507796
GWAS Ctlgrs397507796
Max Magnitude6
ClinVar
Risk rs397507796(-;-)
Alt rs397507796(-;-)
Reference Rs397507796(A;A)
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.32914157delA
CLNSRC ClinVar
CLNACC RCV000044715.2, RCV000257697.2,