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rs587776636

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776636(-;-)
Make rs587776636(-;A)
Make rs587776636(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85267931
GeneBCL10
is asnp
is mentioned by
dbSNPrs587776636
ebirs587776636
HLIrs587776636
Exacrs587776636
Varsomers587776636
Maprs587776636
PheGenIrs587776636
hapmaprs587776636
1000 genomesrs587776636
hgdprs587776636
ensemblrs587776636
gopubmedrs587776636
geneviewrs587776636
scholarrs587776636
googlers587776636
pharmgkbrs587776636
gwascentralrs587776636
openSNPrs587776636
23andMers587776636
23andMe allrs587776636
SNP Nexus

SNPshotrs587776636
SNPdbers587776636
MSV3drs587776636
GWAS Ctlgrs587776636
Max Magnitude0
ClinVar
Risk rs587776636(A;A)
Alt rs587776636(A;A)
Reference rs587776636(;)
Significance Pathogenic
Disease Follicular lymphoma
Variation info
Gene BCL10
CLNDBN Follicular lymphoma
Reversed 0
HGVS NC_000001.10:g.85733614dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000006635.5,