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

rs879255295

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255295(-;-)
Make rs879255295(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43070938
GeneBRCA1
is asnp
is mentioned by
dbSNPrs879255295
ebirs879255295
HLIrs879255295
Exacrs879255295
Varsomers879255295
Maprs879255295
PheGenIrs879255295
hapmaprs879255295
1000 genomesrs879255295
hgdprs879255295
ensemblrs879255295
gopubmedrs879255295
geneviewrs879255295
scholarrs879255295
googlers879255295
pharmgkbrs879255295
gwascentralrs879255295
openSNPrs879255295
23andMers879255295
23andMe allrs879255295
SNP Nexus

SNPshotrs879255295
SNPdbers879255295
MSV3drs879255295
GWAS Ctlgrs879255295
Max Magnitude0
ClinVar
Risk rs879255295(;)
Alt rs879255295(;)
Reference rs879255295(C;C)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41222955delG
CLNSRC
CLNACC RCV000239129.1,