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rs397507922

From SNPedia

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


Make rs397507922(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356610
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507922
ebirs397507922
HLIrs397507922
Exacrs397507922
Varsomers397507922
Maprs397507922
PheGenIrs397507922
hapmaprs397507922
1000 genomesrs397507922
hgdprs397507922
ensemblrs397507922
gopubmedrs397507922
geneviewrs397507922
scholarrs397507922
googlers397507922
pharmgkbrs397507922
gwascentralrs397507922
openSNPrs397507922
23andMers397507922
23andMe allrs397507922
SNP Nexus

SNPshotrs397507922
SNPdbers397507922
MSV3drs397507922
GWAS Ctlgrs397507922
Max Magnitude6
ClinVar
Risk rs397507922(A,T;A,T)
Alt rs397507922(A,T;A,T)
Reference rs397507922(G;G)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not provided Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 not provided Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32930747G>A; NC_000013.10:g.32930747G>C; NC_000013.10:g.32930747G>T
CLNSRC ClinVar
CLNACC RCV000045259.3, RCV000083138.3, RCV000235926.1, RCV000045260.2,