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rs397507932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507932(-;-)
Make rs397507932(-;T)
Make rs397507932(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357804
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507932
ebirs397507932
HLIrs397507932
Exacrs397507932
Varsomers397507932
Maprs397507932
PheGenIrs397507932
hapmaprs397507932
1000 genomesrs397507932
hgdprs397507932
ensemblrs397507932
gopubmedrs397507932
geneviewrs397507932
scholarrs397507932
googlers397507932
pharmgkbrs397507932
gwascentralrs397507932
openSNPrs397507932
23andMers397507932
23andMe allrs397507932
SNP Nexus

SNPshotrs397507932
SNPdbers397507932
MSV3drs397507932
GWAS Ctlgrs397507932
Max Magnitude0
ClinVar
Risk rs397507932(T;T)
Alt rs397507932(T;T)
Reference rs397507932(;)
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.32931941dupT
CLNSRC ClinVar
CLNACC RCV000045285.2, RCV000082977.2,