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rs10264784

From SNPedia

Associated with end-of-induction minimal risidual disease (MRD) in childhood acute lymphoblastic leukemia (ALL) from 2 independent cohorts (GWAS result). Risk Allele: C, MAF= 0.17, combined P value= 3.79E-04.
Orientationplus
Stabilizedplus
Make rs10264784(C;C)
Make rs10264784(C;T)
Make rs10264784(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position19869907
is asnp
is mentioned by
dbSNPrs10264784
ebirs10264784
HLIrs10264784
Exacrs10264784
Varsomers10264784
Maprs10264784
PheGenIrs10264784
hapmaprs10264784
1000 genomesrs10264784
hgdprs10264784
ensemblrs10264784
gopubmedrs10264784
geneviewrs10264784
scholarrs10264784
googlers10264784
pharmgkbrs10264784
gwascentralrs10264784
openSNPrs10264784
23andMers10264784
23andMe allrs10264784
SNP Nexus

SNPshotrs10264784
SNPdbers10264784
MSV3drs10264784
GWAS Ctlgrs10264784
GMAF0.2663
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs10264784
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.273438
summary