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rs876658593

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658593(G;T)
Make rs876658593(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092812
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658593
ebirs876658593
HLIrs876658593
Exacrs876658593
Varsomers876658593
Maprs876658593
PheGenIrs876658593
hapmaprs876658593
1000 genomesrs876658593
hgdprs876658593
ensemblrs876658593
gopubmedrs876658593
geneviewrs876658593
scholarrs876658593
googlers876658593
pharmgkbrs876658593
gwascentralrs876658593
openSNPrs876658593
23andMers876658593
23andMe allrs876658593
SNP Nexus

SNPshotrs876658593
SNPdbers876658593
MSV3drs876658593
GWAS Ctlgrs876658593
Max Magnitude0
ClinVar
Risk rs876658593(T;T)
Alt rs876658593(T;T)
Reference rs876658593(G;G)
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.41244829C>A
CLNSRC
CLNACC RCV000220421.1,