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rs10828317

From SNPedia

Merged intors2230469
Orientationminus
Stabilizedminus
Make rs10828317(A;A)
Make rs10828317(A;G)
Make rs10828317(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position22550699
GenePIP4K2A
is asnp
is mentioned by
dbSNPrs10828317
ebirs10828317
HLIrs10828317
Exacrs10828317
Varsomers10828317
Maprs10828317
PheGenIrs10828317
hapmaprs10828317
1000 genomesrs10828317
hgdprs10828317
ensemblrs10828317
gopubmedrs10828317
geneviewrs10828317
scholarrs10828317
googlers10828317
pharmgkbrs10828317
gwascentralrs10828317
openSNPrs10828317
23andMers10828317
23andMe allrs10828317
SNP Nexus

SNPshotrs10828317
SNPdbers10828317
MSV3drs10828317
GWAS Ctlgrs10828317
StatusMerged into rs2230469
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23996088]
Trait Acute lymphoblastic leukemia (B-cell precursor)
Title Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype.
Risk Allele T
P-val 2E-9
Odds Ratio 1.23 [1.15-1.32]