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rs876659614

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659614(C;T)
Make rs876659614(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43099880
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659614
ebirs876659614
HLIrs876659614
Exacrs876659614
Varsomers876659614
Maprs876659614
PheGenIrs876659614
hapmaprs876659614
1000 genomesrs876659614
hgdprs876659614
ensemblrs876659614
gopubmedrs876659614
geneviewrs876659614
scholarrs876659614
googlers876659614
pharmgkbrs876659614
gwascentralrs876659614
openSNPrs876659614
23andMers876659614
23andMe allrs876659614
SNP Nexus

SNPshotrs876659614
SNPdbers876659614
MSV3drs876659614
GWAS Ctlgrs876659614
Max Magnitude0
ClinVar
Risk rs876659614(A,T;A,T)
Alt rs876659614(A,T;A,T)
Reference rs876659614(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41251897G>A; NC_000017.10:g.41251897G>T
CLNSRC
CLNACC RCV000219699.1, RCV000238612.1, RCV000214368.1,