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rs17756311

From SNPedia

Linked to childhood acute lymphoblastic leukemia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1.5 Possible higher risk of childhood acute lymphoblastic leukemia
Make rs17756311(A;G)
Make rs17756311(G;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position22053896
GeneCDKN2B-AS1
is asnp
is mentioned by
dbSNPrs17756311
ebirs17756311
HLIrs17756311
Exacrs17756311
Varsomers17756311
Maprs17756311
PheGenIrs17756311
hapmaprs17756311
1000 genomesrs17756311
hgdprs17756311
ensemblrs17756311
gopubmedrs17756311
geneviewrs17756311
scholarrs17756311
googlers17756311
pharmgkbrs17756311
gwascentralrs17756311
openSNPrs17756311
23andMers17756311
23andMe allrs17756311
SNP Nexus

SNPshotrs17756311
SNPdbers17756311
MSV3drs17756311
GWAS Ctlgrs17756311
Max Magnitude1.5
? (A;A) (A;G) (G;G) 28
[PMID 23512250OA-icon.png] Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations.