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rs397507902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar
Make rs397507902(A;A)
Make rs397507902(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319080
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507902
dbSNP (old)rs397507902
ClinGenrs397507902
ebirs397507902
HLIrs397507902
Exacrs397507902
Gnomadrs397507902
Varsomers397507902
Maprs397507902
PheGenIrs397507902
Biobankrs397507902
1000 genomesrs397507902
hgdprs397507902
ensemblrs397507902
gopubmedrs397507902
geneviewrs397507902
scholarrs397507902
googlers397507902
pharmgkbrs397507902
gwascentralrs397507902
openSNPrs397507902
23andMers397507902
23andMe allrs397507902
SNP Nexus

SNPshotrs397507902
SNPdbers397507902
MSV3drs397507902
GWAS Ctlgrs397507902
Max Magnitude6
ClinVar
Risk rs397507902(A;A) rs397507902(G;G)
Alt rs397507902(A;A) rs397507902(G;G)
Reference Rs397507902(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.32893217T>A; NC_000013.10:g.32893217T>G
CLNSRC ClinVar
CLNACC RCV000045162.2, RCV000257036.2,