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rs10170236

From SNPedia

Orientationplus
Stabilizedplus
Make rs10170236(A;A)
Make rs10170236(A;G)
Make rs10170236(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position149601110
GeneAC144449.1
is asnp
is mentioned by
dbSNPrs10170236
ebirs10170236
HLIrs10170236
Exacrs10170236
Varsomers10170236
Maprs10170236
PheGenIrs10170236
hapmaprs10170236
1000 genomesrs10170236
hgdprs10170236
ensemblrs10170236
gopubmedrs10170236
geneviewrs10170236
scholarrs10170236
googlers10170236
pharmgkbrs10170236
gwascentralrs10170236
openSNPrs10170236
23andMers10170236
23andMe allrs10170236
SNP Nexus

SNPshotrs10170236
SNPdbers10170236
MSV3drs10170236
GWAS Ctlgrs10170236
GMAF0.3104
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23007406OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Risk Allele C
P-val 4E-6
Odds Ratio 1.45 [1.24-1.69]