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

rs587776637

From SNPedia

Orientationplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs587776637(-;-)
Make rs587776637(-;CTT)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85267692
GeneBCL10
is asnp
is mentioned by
dbSNPrs587776637
ebirs587776637
HLIrs587776637
Exacrs587776637
Varsomers587776637
Maprs587776637
PheGenIrs587776637
hapmaprs587776637
1000 genomesrs587776637
hgdprs587776637
ensemblrs587776637
gopubmedrs587776637
geneviewrs587776637
scholarrs587776637
googlers587776637
pharmgkbrs587776637
gwascentralrs587776637
openSNPrs587776637
23andMers587776637
23andMe allrs587776637
SNP Nexus

SNPshotrs587776637
SNPdbers587776637
MSV3drs587776637
GWAS Ctlgrs587776637
Max Magnitude0
ClinVar
Risk rs587776637(;)
Alt rs587776637(;)
Reference rs587776637(CTT;CTT)
Significance Pathogenic
Disease Follicular lymphoma
Variation info
Gene BCL10
CLNDBN Follicular lymphoma
Reversed 0
HGVS NC_000001.10:g.85733375_85733377delCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006636.5,