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rs587776631

From SNPedia

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Geno Mag Summary
(AG;AG) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776631(-;-)
Make rs587776631(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85270619
GeneBCL10
is asnp
is mentioned by
dbSNPrs587776631
ebirs587776631
HLIrs587776631
Exacrs587776631
Varsomers587776631
Maprs587776631
PheGenIrs587776631
hapmaprs587776631
1000 genomesrs587776631
hgdprs587776631
ensemblrs587776631
gopubmedrs587776631
geneviewrs587776631
scholarrs587776631
googlers587776631
pharmgkbrs587776631
gwascentralrs587776631
openSNPrs587776631
23andMers587776631
23andMe allrs587776631
SNP Nexus

SNPshotrs587776631
SNPdbers587776631
MSV3drs587776631
GWAS Ctlgrs587776631
Max Magnitude0
ClinVar
Risk rs587776631(TG,G;TG,G)
Alt rs587776631(TG,G;TG,G)
Reference rs587776631(AG;AG)
Significance Pathogenic
Disease Mucosa-associated lymphoma
Variation info
Gene BCL10
CLNDBN Mucosa-associated lymphoma
Reversed 1
HGVS NC_000001.10:g.85736302delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006630.4,