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rs878853296

From SNPedia

Orientationminus
Geno Mag Summary
(GGTG;GGTG) 0 common in clinvar
Make rs878853296(-;-)
Make rs878853296(-;GGTG)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43045771
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878853296
ebirs878853296
HLIrs878853296
Exacrs878853296
Varsomers878853296
Maprs878853296
PheGenIrs878853296
hapmaprs878853296
1000 genomesrs878853296
hgdprs878853296
ensemblrs878853296
gopubmedrs878853296
geneviewrs878853296
scholarrs878853296
googlers878853296
pharmgkbrs878853296
gwascentralrs878853296
openSNPrs878853296
23andMers878853296
23andMe allrs878853296
SNP Nexus

SNPshotrs878853296
SNPdbers878853296
MSV3drs878853296
GWAS Ctlgrs878853296
Max Magnitude0
ClinVar
Risk rs878853296(;)
Alt rs878853296(;)
Reference rs878853296(GGTG;GGTG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41197788_41197791delCACC
CLNSRC
CLNACC RCV000225437.1,