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rs587776879

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776879(C;C)
Make rs587776879(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position52407318
GeneBAP1
is asnp
is mentioned by
dbSNPrs587776879
ebirs587776879
HLIrs587776879
Exacrs587776879
Varsomers587776879
Maprs587776879
PheGenIrs587776879
hapmaprs587776879
1000 genomesrs587776879
hgdprs587776879
ensemblrs587776879
gopubmedrs587776879
geneviewrs587776879
scholarrs587776879
googlers587776879
pharmgkbrs587776879
gwascentralrs587776879
openSNPrs587776879
23andMers587776879
23andMe allrs587776879
SNP Nexus

SNPshotrs587776879
SNPdbers587776879
MSV3drs587776879
GWAS Ctlgrs587776879
Max Magnitude0
ClinVar
Risk rs587776879(C,T;C,T)
Alt rs587776879(C,T;C,T)
Reference rs587776879(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BAP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000003.11:g.52441334T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023236.2,