Have questions? Visit https://www.reddit.com/r/SNPedia

rs879255309

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255309(C;T)
Make rs879255309(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338238
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255309
ebirs879255309
HLIrs879255309
Exacrs879255309
Varsomers879255309
Maprs879255309
PheGenIrs879255309
hapmaprs879255309
1000 genomesrs879255309
hgdprs879255309
ensemblrs879255309
gopubmedrs879255309
geneviewrs879255309
scholarrs879255309
googlers879255309
pharmgkbrs879255309
gwascentralrs879255309
openSNPrs879255309
23andMers879255309
23andMe allrs879255309
SNP Nexus

SNPshotrs879255309
SNPdbers879255309
MSV3drs879255309
GWAS Ctlgrs879255309
Max Magnitude0
ClinVar
Risk rs879255309(T;T)
Alt rs879255309(T;T)
Reference rs879255309(C;C)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912375C>T
CLNSRC
CLNACC RCV000239260.1,