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rs876659533

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659533(C;T)
Make rs876659533(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61776445
GeneBRIP1
is asnp
is mentioned by
dbSNPrs876659533
ebirs876659533
HLIrs876659533
Exacrs876659533
Varsomers876659533
Maprs876659533
PheGenIrs876659533
hapmaprs876659533
1000 genomesrs876659533
hgdprs876659533
ensemblrs876659533
gopubmedrs876659533
geneviewrs876659533
scholarrs876659533
googlers876659533
pharmgkbrs876659533
gwascentralrs876659533
openSNPrs876659533
23andMers876659533
23andMe allrs876659533
SNP Nexus

SNPshotrs876659533
SNPdbers876659533
MSV3drs876659533
GWAS Ctlgrs876659533
Max Magnitude0
ClinVar
Risk rs876659533(T;T)
Alt rs876659533(T;T)
Reference rs876659533(C;C)
Significance 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.59853806G>A
CLNSRC
CLNACC RCV000223392.1,