Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776633

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776633(-;-)
Make rs587776633(-;T)
Make rs587776633(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85270733
GeneBCL10
is asnp
is mentioned by
dbSNPrs587776633
ebirs587776633
HLIrs587776633
Exacrs587776633
Varsomers587776633
Maprs587776633
PheGenIrs587776633
hapmaprs587776633
1000 genomesrs587776633
hgdprs587776633
ensemblrs587776633
gopubmedrs587776633
geneviewrs587776633
scholarrs587776633
googlers587776633
pharmgkbrs587776633
gwascentralrs587776633
openSNPrs587776633
23andMers587776633
23andMe allrs587776633
SNP Nexus

SNPshotrs587776633
SNPdbers587776633
MSV3drs587776633
GWAS Ctlgrs587776633
Max Magnitude0
ClinVar
Risk rs587776633(T;T)
Alt rs587776633(T;T)
Reference rs587776633(;)
Significance Pathogenic
Disease Follicular lymphoma
Variation info
Gene BCL10
CLNDBN Follicular lymphoma
Reversed 0
HGVS NC_000001.10:g.85736416dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006632.5,