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. |
Orientation | plus |
Stabilized | plus |
Make rs10264784(C;C) |
Make rs10264784(C;T) |
Make rs10264784(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 19869907 |
is a | snp |
is | mentioned by |
dbSNP | rs10264784 |
dbSNP (classic) | rs10264784 |
ClinGen | rs10264784 |
ebi | rs10264784 |
HLI | rs10264784 |
Exac | rs10264784 |
Gnomad | rs10264784 |
Varsome | rs10264784 |
LitVar | rs10264784 |
Map | rs10264784 |
PheGenI | rs10264784 |
Biobank | rs10264784 |
1000 genomes | rs10264784 |
hgdp | rs10264784 |
ensembl | rs10264784 |
geneview | rs10264784 |
scholar | rs10264784 |
rs10264784 | |
pharmgkb | rs10264784 |
gwascentral | rs10264784 |
openSNP | rs10264784 |
23andMe | rs10264784 |
SNPshot | rs10264784 |
SNPdbe | rs10264784 |
MSV3d | rs10264784 |
GWAS Ctlg | rs10264784 |
GMAF | 0.2663 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
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