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

rs879255293

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879255293(G;G)
Make rs879255293(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43074329
GeneBRCA1
is asnp
is mentioned by
dbSNPrs879255293
ebirs879255293
HLIrs879255293
Exacrs879255293
Varsomers879255293
Maprs879255293
PheGenIrs879255293
hapmaprs879255293
1000 genomesrs879255293
hgdprs879255293
ensemblrs879255293
gopubmedrs879255293
geneviewrs879255293
scholarrs879255293
googlers879255293
pharmgkbrs879255293
gwascentralrs879255293
openSNPrs879255293
23andMers879255293
23andMe allrs879255293
SNP Nexus

SNPshotrs879255293
SNPdbers879255293
MSV3drs879255293
GWAS Ctlgrs879255293
Max Magnitude0
ClinVar
Risk rs879255293(G;G)
Alt rs879255293(G;G)
Reference rs879255293(T;T)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41226346A>C
CLNSRC
CLNACC RCV000239340.1,