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rs876658626

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658626(-;-)
Make rs876658626(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092237
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658626
ebirs876658626
HLIrs876658626
Exacrs876658626
Varsomers876658626
Maprs876658626
PheGenIrs876658626
hapmaprs876658626
1000 genomesrs876658626
hgdprs876658626
ensemblrs876658626
gopubmedrs876658626
geneviewrs876658626
scholarrs876658626
googlers876658626
pharmgkbrs876658626
gwascentralrs876658626
openSNPrs876658626
23andMers876658626
23andMe allrs876658626
SNP Nexus

SNPshotrs876658626
SNPdbers876658626
MSV3drs876658626
GWAS Ctlgrs876658626
Max Magnitude0
ClinVar
Risk rs876658626(;)
Alt rs876658626(;)
Reference rs876658626(T;T)
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.41244254delA
CLNSRC
CLNACC RCV000216850.1,