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rs397507686

From SNPedia

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


Make rs397507686(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338133
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507686
dbSNP (old)rs397507686
ClinGenrs397507686
ebirs397507686
HLIrs397507686
Exacrs397507686
Varsomers397507686
Maprs397507686
PheGenIrs397507686
Biobankrs397507686
1000 genomesrs397507686
hgdprs397507686
ensemblrs397507686
gopubmedrs397507686
geneviewrs397507686
scholarrs397507686
googlers397507686
pharmgkbrs397507686
gwascentralrs397507686
openSNPrs397507686
23andMers397507686
23andMe allrs397507686
SNP Nexus

SNPshotrs397507686
SNPdbers397507686
MSV3drs397507686
GWAS Ctlgrs397507686
Max Magnitude6
ClinVar
Risk rs397507686(-;-)
Alt rs397507686(-;-)
Reference Rs397507686(TT;TT)
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.32912270_32912271delTT
CLNSRC ClinVar
CLNACC RCV000044264.2, RCV000256856.2,