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rs431825362

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs431825362(A;A)
Make rs431825362(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32363187
GeneBRCA2
is asnp
is mentioned by
dbSNPrs431825362
dbSNP (old)rs431825362
ClinGenrs431825362
ebirs431825362
HLIrs431825362
Exacrs431825362
Gnomadrs431825362
Varsomers431825362
Maprs431825362
PheGenIrs431825362
Biobankrs431825362
1000 genomesrs431825362
hgdprs431825362
ensemblrs431825362
gopubmedrs431825362
geneviewrs431825362
scholarrs431825362
googlers431825362
pharmgkbrs431825362
gwascentralrs431825362
openSNPrs431825362
23andMers431825362
23andMe allrs431825362
SNP Nexus

SNPshotrs431825362
SNPdbers431825362
MSV3drs431825362
GWAS Ctlgrs431825362
Max Magnitude0
ClinVar
Risk rs431825362(A;A) rs431825362(T;T)
Alt rs431825362(A;A) rs431825362(T;T)
Reference Rs431825362(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not specified
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 not specified
Reversed 0
HGVS NC_000013.10:g.32937324C>A; NC_000013.10:g.32937324C>T
CLNSRC
CLNACC RCV000082985.2, RCV000129687.3, RCV000196144.2, RCV000210092.1, RCV000278676.1, RCV000163213.2, RCV000216858.2, RCV000465103.1,