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rs397507649

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar
Make rs397507649(A;A)
Make rs397507649(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337345
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507649
dbSNP (old)rs397507649
ClinGenrs397507649
ebirs397507649
HLIrs397507649
Exacrs397507649
Gnomadrs397507649
Varsomers397507649
Maprs397507649
PheGenIrs397507649
Biobankrs397507649
1000 genomesrs397507649
hgdprs397507649
ensemblrs397507649
gopubmedrs397507649
geneviewrs397507649
scholarrs397507649
googlers397507649
pharmgkbrs397507649
gwascentralrs397507649
openSNPrs397507649
23andMers397507649
23andMe allrs397507649
SNP Nexus

SNPshotrs397507649
SNPdbers397507649
MSV3drs397507649
GWAS Ctlgrs397507649
Max Magnitude6
ClinVar
Risk rs397507649(A;A) rs397507649(G;G)
Alt rs397507649(A;A) rs397507649(G;G)
Reference Rs397507649(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.32911482T>A; NC_000013.10:g.32911482T>G
CLNSRC ClinVar
CLNACC RCV000044100.2, RCV000256883.2,