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

rs879255315

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879255315(A;T)
Make rs879255315(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092548
GeneBRCA1
is asnp
is mentioned by
dbSNPrs879255315
ebirs879255315
HLIrs879255315
Exacrs879255315
Varsomers879255315
Maprs879255315
PheGenIrs879255315
hapmaprs879255315
1000 genomesrs879255315
hgdprs879255315
ensemblrs879255315
gopubmedrs879255315
geneviewrs879255315
scholarrs879255315
googlers879255315
pharmgkbrs879255315
gwascentralrs879255315
openSNPrs879255315
23andMers879255315
23andMe allrs879255315
SNP Nexus

SNPshotrs879255315
SNPdbers879255315
MSV3drs879255315
GWAS Ctlgrs879255315
Max Magnitude0
ClinVar
Risk rs879255315(T;T)
Alt rs879255315(T;T)
Reference rs879255315(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA1
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.41244565T>A
CLNSRC
CLNACC RCV000238695.1,