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rs876659707

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659707(A;T)
Make rs876659707(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61847222
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876659707
ebirs876659707
HLIrs876659707
Exacrs876659707
Varsomers876659707
Maprs876659707
PheGenIrs876659707
hapmaprs876659707
1000 genomesrs876659707
hgdprs876659707
ensemblrs876659707
gopubmedrs876659707
geneviewrs876659707
scholarrs876659707
googlers876659707
pharmgkbrs876659707
gwascentralrs876659707
openSNPrs876659707
23andMers876659707
23andMe allrs876659707
SNP Nexus

SNPshotrs876659707
SNPdbers876659707
MSV3drs876659707
GWAS Ctlgrs876659707
Max Magnitude0
ClinVar
Risk rs876659707(T;T)
Alt rs876659707(T;T)
Reference rs876659707(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.59924583T>A
CLNSRC
CLNACC RCV000214929.1,