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rs587776638

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs587776638(-;-)
Make rs587776638(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85267901
GeneBCL10
is asnp
is mentioned by
dbSNPrs587776638
ebirs587776638
HLIrs587776638
Exacrs587776638
Varsomers587776638
Maprs587776638
PheGenIrs587776638
hapmaprs587776638
1000 genomesrs587776638
hgdprs587776638
ensemblrs587776638
gopubmedrs587776638
geneviewrs587776638
scholarrs587776638
googlers587776638
pharmgkbrs587776638
gwascentralrs587776638
openSNPrs587776638
23andMers587776638
23andMe allrs587776638
SNP Nexus

SNPshotrs587776638
SNPdbers587776638
MSV3drs587776638
GWAS Ctlgrs587776638
Max Magnitude0
ClinVar
Risk rs587776638(AC,C;AC,C)
Alt rs587776638(AC,C;AC,C)
Reference rs587776638(TC;TC)
Significance Pathogenic
Disease Sezary syndrome
Variation info
Gene BCL10
CLNDBN Sezary syndrome
Reversed 1
HGVS NC_000001.10:g.85733584delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000006638.4,