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rs878853289

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853289(-;-)
Make rs878853289(-;CC)
Make rs878853289(CC;CC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093649
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878853289
ebirs878853289
HLIrs878853289
Exacrs878853289
Varsomers878853289
Maprs878853289
PheGenIrs878853289
hapmaprs878853289
1000 genomesrs878853289
hgdprs878853289
ensemblrs878853289
gopubmedrs878853289
geneviewrs878853289
scholarrs878853289
googlers878853289
pharmgkbrs878853289
gwascentralrs878853289
openSNPrs878853289
23andMers878853289
23andMe allrs878853289
SNP Nexus

SNPshotrs878853289
SNPdbers878853289
MSV3drs878853289
GWAS Ctlgrs878853289
Max Magnitude0
ClinVar
Risk rs878853289(CC;CC)
Alt rs878853289(CC;CC)
Reference rs878853289(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41245666_41245667insGG
CLNSRC
CLNACC RCV000225660.1,