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rs387906351

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906351(-;-)
Make rs387906351(-;A)
Make rs387906351(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85270827
GeneBCL10
is asnp
is mentioned by
dbSNPrs387906351
ebirs387906351
HLIrs387906351
Exacrs387906351
Varsomers387906351
Maprs387906351
PheGenIrs387906351
hapmaprs387906351
1000 genomesrs387906351
hgdprs387906351
ensemblrs387906351
gopubmedrs387906351
geneviewrs387906351
scholarrs387906351
googlers387906351
pharmgkbrs387906351
gwascentralrs387906351
openSNPrs387906351
23andMers387906351
23andMe allrs387906351
SNP Nexus

SNPshotrs387906351
SNPdbers387906351
MSV3drs387906351
GWAS Ctlgrs387906351
Max Magnitude0
ClinVar
Risk rs387906351(A;A)
Alt rs387906351(A;A)
Reference rs387906351(;)
Significance Pathogenic
Disease T-cell acute lymphoblastic leukemia Carcinoma of colon
Variation info
Gene BCL10
CLNDBN T-cell acute lymphoblastic leukemia Carcinoma of colon
Reversed 1
HGVS NC_000001.10:g.85736511dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006637.4, RCV000023308.4,