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rs397508025

From SNPedia

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


Make rs397508025(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379774
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508025
dbSNP (old)rs397508025
ClinGenrs397508025
ebirs397508025
HLIrs397508025
Exacrs397508025
Varsomers397508025
Maprs397508025
PheGenIrs397508025
Biobankrs397508025
1000 genomesrs397508025
hgdprs397508025
ensemblrs397508025
gopubmedrs397508025
geneviewrs397508025
scholarrs397508025
googlers397508025
pharmgkbrs397508025
gwascentralrs397508025
openSNPrs397508025
23andMers397508025
23andMe allrs397508025
SNP Nexus

SNPshotrs397508025
SNPdbers397508025
MSV3drs397508025
GWAS Ctlgrs397508025
Max Magnitude6
ClinVar
Risk rs397508025(A;A) rs397508025(G;G)
Alt rs397508025(A;A) rs397508025(G;G)
Reference Rs397508025(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32953911C>A; NC_000013.10:g.32953911C>G
CLNSRC ClinVar
CLNACC RCV000045677.2, RCV000256867.2, RCV000160161.2, RCV000221983.1, RCV000241294.1,