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rs397507801

From SNPedia

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


Make rs397507801(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340094
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507801
dbSNP (old)rs397507801
ClinGenrs397507801
ebirs397507801
HLIrs397507801
Exacrs397507801
Gnomadrs397507801
Varsomers397507801
Maprs397507801
PheGenIrs397507801
Biobankrs397507801
1000 genomesrs397507801
hgdprs397507801
ensemblrs397507801
gopubmedrs397507801
geneviewrs397507801
scholarrs397507801
googlers397507801
pharmgkbrs397507801
gwascentralrs397507801
openSNPrs397507801
23andMers397507801
23andMe allrs397507801
SNP Nexus

SNPshotrs397507801
SNPdbers397507801
MSV3drs397507801
GWAS Ctlgrs397507801
Max Magnitude6
ClinVar
Risk rs397507801(A;A)
Alt rs397507801(A;A)
Reference Rs397507801(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.32914231T>A
CLNSRC ClinVar
CLNACC RCV000044739.2, RCV000241195.1,