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rs587776639

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776639(-;-)
Make rs587776639(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85270828
GeneBCL10
is asnp
is mentioned by
dbSNPrs587776639
ClinGenrs587776639
ebirs587776639
HLIrs587776639
Exacrs587776639
Varsomers587776639
Maprs587776639
PheGenIrs587776639
hapmaprs587776639
1000 genomesrs587776639
hgdprs587776639
ensemblrs587776639
gopubmedrs587776639
geneviewrs587776639
scholarrs587776639
googlers587776639
pharmgkbrs587776639
gwascentralrs587776639
openSNPrs587776639
23andMers587776639
23andMe allrs587776639
SNP Nexus

SNPshotrs587776639
SNPdbers587776639
MSV3drs587776639
GWAS Ctlgrs587776639
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs587776639(T;T)
Significance Pathogenic
Disease Mesothelioma
Variation info
Gene BCL10
CLNDBN Mesothelioma
Reversed 0
HGVS NC_000001.10:g.85736511delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006641.5,