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rs587776632

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776632(-;-)
Make rs587776632(-;AA)
Make rs587776632(AA;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85267902
GeneBCL10
is asnp
is mentioned by
dbSNPrs587776632
ebirs587776632
HLIrs587776632
Exacrs587776632
Varsomers587776632
Maprs587776632
PheGenIrs587776632
hapmaprs587776632
1000 genomesrs587776632
hgdprs587776632
ensemblrs587776632
gopubmedrs587776632
geneviewrs587776632
scholarrs587776632
googlers587776632
pharmgkbrs587776632
gwascentralrs587776632
openSNPrs587776632
23andMers587776632
23andMe allrs587776632
SNP Nexus

SNPshotrs587776632
SNPdbers587776632
MSV3drs587776632
GWAS Ctlgrs587776632
Max Magnitude0
ClinVar
Risk rs587776632(AA;AA)
Alt rs587776632(AA;AA)
Reference rs587776632(;)
Significance Pathogenic
Disease Follicular lymphoma
Variation info
Gene BCL10
CLNDBN Follicular lymphoma
Reversed 0
HGVS NC_000001.10:g.85733584_85733585dupAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000006631.5,