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rs142899125

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs142899125(A;G)
Make rs142899125(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362582
GeneBRCA2
is asnp
is mentioned by
dbSNPrs142899125
ebirs142899125
HLIrs142899125
Exacrs142899125
Varsomers142899125
Maprs142899125
PheGenIrs142899125
hapmaprs142899125
1000 genomesrs142899125
hgdprs142899125
ensemblrs142899125
gopubmedrs142899125
geneviewrs142899125
scholarrs142899125
googlers142899125
pharmgkbrs142899125
gwascentralrs142899125
openSNPrs142899125
23andMers142899125
23andMe allrs142899125
SNP Nexus

SNPshotrs142899125
SNPdbers142899125
MSV3drs142899125
GWAS Ctlgrs142899125
Max Magnitude0
ClinVar
Risk rs142899125(G;G)
Alt rs142899125(G;G)
Reference rs142899125(A;A)
Significance Other
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified not provided Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified not provided Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32936719A>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000077013.3, RCV000130086.2, RCV000160144.2, RCV000175118.1, RCV000197898.1,