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rs397507632

From SNPedia

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


Make rs397507632(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336944
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507632
dbSNP (old)rs397507632
ClinGenrs397507632
ebirs397507632
HLIrs397507632
Exacrs397507632
Varsomers397507632
Maprs397507632
PheGenIrs397507632
Biobankrs397507632
1000 genomesrs397507632
hgdprs397507632
ensemblrs397507632
gopubmedrs397507632
geneviewrs397507632
scholarrs397507632
googlers397507632
pharmgkbrs397507632
gwascentralrs397507632
openSNPrs397507632
23andMers397507632
23andMe allrs397507632
SNP Nexus

SNPshotrs397507632
SNPdbers397507632
MSV3drs397507632
GWAS Ctlgrs397507632
Max Magnitude6
ClinVar
Risk rs397507632(-;-)
Alt rs397507632(-;-)
Reference Rs397507632(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.32911081delT
CLNSRC ClinVar
CLNACC RCV000044021.2, RCV000241432.1,