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rs879255317

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs879255317(-;-)
Make rs879255317(-;CA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43076599
GeneBRCA1
is asnp
is mentioned by
dbSNPrs879255317
ebirs879255317
HLIrs879255317
Exacrs879255317
Varsomers879255317
Maprs879255317
PheGenIrs879255317
hapmaprs879255317
1000 genomesrs879255317
hgdprs879255317
ensemblrs879255317
gopubmedrs879255317
geneviewrs879255317
scholarrs879255317
googlers879255317
pharmgkbrs879255317
gwascentralrs879255317
openSNPrs879255317
23andMers879255317
23andMe allrs879255317
SNP Nexus

SNPshotrs879255317
SNPdbers879255317
MSV3drs879255317
GWAS Ctlgrs879255317
Max Magnitude0
ClinVar
Risk rs879255317(;)
Alt rs879255317(;)
Reference rs879255317(CA;CA)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41228616_41228617delTG
CLNSRC
CLNACC RCV000238997.1,