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rs879255316

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879255316(-;-)
Make rs879255316(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092399
GeneBRCA1
is asnp
is mentioned by
dbSNPrs879255316
ebirs879255316
HLIrs879255316
Exacrs879255316
Varsomers879255316
Maprs879255316
PheGenIrs879255316
hapmaprs879255316
1000 genomesrs879255316
hgdprs879255316
ensemblrs879255316
gopubmedrs879255316
geneviewrs879255316
scholarrs879255316
googlers879255316
pharmgkbrs879255316
gwascentralrs879255316
openSNPrs879255316
23andMers879255316
23andMe allrs879255316
SNP Nexus

SNPshotrs879255316
SNPdbers879255316
MSV3drs879255316
GWAS Ctlgrs879255316
Max Magnitude0
ClinVar
Risk rs879255316(;)
Alt rs879255316(;)
Reference rs879255316(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA1
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.41244416delA
CLNSRC
CLNACC RCV000238875.1,