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rs587776635

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776635(-;-)
Make rs587776635(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85267919
GeneBCL10
is asnp
is mentioned by
dbSNPrs587776635
ebirs587776635
HLIrs587776635
Exacrs587776635
Varsomers587776635
Maprs587776635
PheGenIrs587776635
hapmaprs587776635
1000 genomesrs587776635
hgdprs587776635
ensemblrs587776635
gopubmedrs587776635
geneviewrs587776635
scholarrs587776635
googlers587776635
pharmgkbrs587776635
gwascentralrs587776635
openSNPrs587776635
23andMers587776635
23andMe allrs587776635
SNP Nexus

SNPshotrs587776635
SNPdbers587776635
MSV3drs587776635
GWAS Ctlgrs587776635
Max Magnitude0
ClinVar
Risk rs587776635(TT;TT) Rs587776635(T;T)
Alt rs587776635(TT;TT) Rs587776635(T;T)
Reference Rs587776635(AT;AT)
Significance Pathogenic
Disease Follicular lymphoma
Variation info
Gene BCL10
CLNDBN Follicular lymphoma
Reversed 1
HGVS NC_000001.10:g.85733602delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006634.6,