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rs876660558

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660558(A;A)
Make rs876660558(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094376
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660558
ebirs876660558
HLIrs876660558
Exacrs876660558
Varsomers876660558
Maprs876660558
PheGenIrs876660558
hapmaprs876660558
1000 genomesrs876660558
hgdprs876660558
ensemblrs876660558
gopubmedrs876660558
geneviewrs876660558
scholarrs876660558
googlers876660558
pharmgkbrs876660558
gwascentralrs876660558
openSNPrs876660558
23andMers876660558
23andMe allrs876660558
SNP Nexus

SNPshotrs876660558
SNPdbers876660558
MSV3drs876660558
GWAS Ctlgrs876660558
Max Magnitude0
ClinVar
Risk rs876660558(A,T;A,T)
Alt rs876660558(A,T;A,T)
Reference rs876660558(G;G)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41246393C>A; NC_000017.10:g.41246393C>T
CLNSRC
CLNACC RCV000226202.1, RCV000239246.1, RCV000215799.1,