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rs397507709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507709(-;-)
Make rs397507709(-;TT)
Make rs397507709(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338495
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507709
ebirs397507709
HLIrs397507709
Exacrs397507709
Varsomers397507709
Maprs397507709
PheGenIrs397507709
hapmaprs397507709
1000 genomesrs397507709
hgdprs397507709
ensemblrs397507709
gopubmedrs397507709
geneviewrs397507709
scholarrs397507709
googlers397507709
pharmgkbrs397507709
gwascentralrs397507709
openSNPrs397507709
23andMers397507709
23andMe allrs397507709
SNP Nexus

SNPshotrs397507709
SNPdbers397507709
MSV3drs397507709
GWAS Ctlgrs397507709
Max Magnitude0
ClinVar
Risk rs397507709(TT;TT)
Alt rs397507709(TT;TT)
Reference rs397507709(;)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32912631_32912632dupTT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044359.2, RCV000113279.1, RCV000130775.2,