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rs879255298

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255298(G;T)
Make rs879255298(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332367
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255298
ebirs879255298
HLIrs879255298
Exacrs879255298
Varsomers879255298
Maprs879255298
PheGenIrs879255298
hapmaprs879255298
1000 genomesrs879255298
hgdprs879255298
ensemblrs879255298
gopubmedrs879255298
geneviewrs879255298
scholarrs879255298
googlers879255298
pharmgkbrs879255298
gwascentralrs879255298
openSNPrs879255298
23andMers879255298
23andMe allrs879255298
SNP Nexus

SNPshotrs879255298
SNPdbers879255298
MSV3drs879255298
GWAS Ctlgrs879255298
Max Magnitude0
ClinVar
Risk rs879255298(T;T)
Alt rs879255298(T;T)
Reference rs879255298(G;G)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32906504G>T
CLNSRC
CLNACC RCV000239093.1,