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rs876659720

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659720(C;T)
Make rs876659720(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43091552
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659720
ebirs876659720
HLIrs876659720
Exacrs876659720
Varsomers876659720
Maprs876659720
PheGenIrs876659720
hapmaprs876659720
1000 genomesrs876659720
hgdprs876659720
ensemblrs876659720
gopubmedrs876659720
geneviewrs876659720
scholarrs876659720
googlers876659720
pharmgkbrs876659720
gwascentralrs876659720
openSNPrs876659720
23andMers876659720
23andMe allrs876659720
SNP Nexus

SNPshotrs876659720
SNPdbers876659720
MSV3drs876659720
GWAS Ctlgrs876659720
Max Magnitude0
ClinVar
Risk rs876659720(T;T)
Alt rs876659720(T;T)
Reference rs876659720(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41243569G>A
CLNSRC
CLNACC RCV000222415.1,