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rs397507389

From SNPedia

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


Make rs397507389(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357741
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507389
dbSNP (old)rs397507389
ClinGenrs397507389
ebirs397507389
HLIrs397507389
Exacrs397507389
Gnomadrs397507389
Varsomers397507389
Maprs397507389
PheGenIrs397507389
Biobankrs397507389
1000 genomesrs397507389
hgdprs397507389
ensemblrs397507389
gopubmedrs397507389
geneviewrs397507389
scholarrs397507389
googlers397507389
pharmgkbrs397507389
gwascentralrs397507389
openSNPrs397507389
23andMers397507389
23andMe allrs397507389
SNP Nexus

SNPshotrs397507389
SNPdbers397507389
MSV3drs397507389
GWAS Ctlgrs397507389
Max Magnitude6
ClinVar
Risk rs397507389(A;A) rs397507389(C;C)
Alt rs397507389(A;A) rs397507389(C;C)
Reference Rs397507389(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32931878G>A; NC_000013.10:g.32931878G>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000031692.5, RCV000045265.6, RCV000131688.3, RCV000195358.3, RCV000474278.1, RCV000045266.2,