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rs587776877

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776877(-;-)
Make rs587776877(-;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position52403840
GeneBAP1
is asnp
is mentioned by
dbSNPrs587776877
ebirs587776877
HLIrs587776877
Exacrs587776877
Varsomers587776877
Maprs587776877
PheGenIrs587776877
hapmaprs587776877
1000 genomesrs587776877
hgdprs587776877
ensemblrs587776877
gopubmedrs587776877
geneviewrs587776877
scholarrs587776877
googlers587776877
pharmgkbrs587776877
gwascentralrs587776877
openSNPrs587776877
23andMers587776877
23andMe allrs587776877
SNP Nexus

SNPshotrs587776877
SNPdbers587776877
MSV3drs587776877
GWAS Ctlgrs587776877
Max Magnitude0
ClinVar
Risk rs587776877(CC,C;CC,C)
Alt rs587776877(CC,C;CC,C)
Reference rs587776877(GC;GC)
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.52437856delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000023234.2,