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rs397507913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507913(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355228
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507913
dbSNP (old)rs397507913
ClinGenrs397507913
ebirs397507913
HLIrs397507913
Exacrs397507913
Gnomadrs397507913
Varsomers397507913
Maprs397507913
PheGenIrs397507913
Biobankrs397507913
1000 genomesrs397507913
hgdprs397507913
ensemblrs397507913
gopubmedrs397507913
geneviewrs397507913
scholarrs397507913
googlers397507913
pharmgkbrs397507913
gwascentralrs397507913
openSNPrs397507913
23andMers397507913
23andMe allrs397507913
SNP Nexus

SNPshotrs397507913
SNPdbers397507913
MSV3drs397507913
GWAS Ctlgrs397507913
Max Magnitude6
ClinVar
Risk rs397507913(T;T)
Alt rs397507913(T;T)
Reference Rs397507913(A;A)
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.32929365A>T
CLNSRC ClinVar
CLNACC RCV000045193.2, RCV000257076.2,