Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3731217
rs3731217
0.030 GeneticVariation BEFREE Here, we conducted a systematic review and meta-analysis to re-evaluate the association of both SNPs (rs3731217 and rs3731249) with ALL susceptibility by gathering the data from 24 independent studies, totally containing 7922 cases/21503 controls for rs3731217 and 6295 cases/24191 controls for rs3731249. 29654170

2018

dbSNP: rs3731249
rs3731249
0.030 GeneticVariation BEFREE Here, we conducted a systematic review and meta-analysis to re-evaluate the association of both SNPs (rs3731217 and rs3731249) with ALL susceptibility by gathering the data from 24 independent studies, totally containing 7922 cases/21503 controls for rs3731217 and 6295 cases/24191 controls for rs3731249. 29654170

2018

dbSNP: rs3731217
rs3731217
0.030 GeneticVariation BEFREE No associations were found between the IKZF1 SNPs (rs11978267; rs7789635), DDC SNPs (rs3779084; rs880028; rs7809758), CDKN2A SNP (rs3731217), the CEBPE SNPs (rs2239633; rs12434881) and LMO1 SNPs (rs442264; rs3794012; rs4237770) with ALL in Yemeni children. 28768142

2017

dbSNP: rs3731249
rs3731249
0.030 GeneticVariation BEFREE The association between rs3731249 genotype and risk was not specific to particular subtype of B-cell ALL. 26463672

2015

dbSNP: rs3731249
rs3731249
0.030 GeneticVariation BEFREE Here we show a missense variant in CDKN2A associated with the development of ALL at genome-wide significance (rs3731249, P=9.4 × 10(-23), odds ratio=2.23). 26104880

2015

dbSNP: rs3731217
rs3731217
0.030 GeneticVariation BEFREE Using data from a genome-wide association study of 907 individuals with childhood acute lymphoblastic leukemia (cases) and 2,398 controls and with validation in samples totaling 2,386 cases and 2,419 controls, we have shown that common variation at 9p21.3 (rs3731217, intron 1 of CDKN2A) influences acute lymphoblastic leukemia risk (odds ratio = 0.71, P = 3.01 x 10(-11)), irrespective of cell lineage. 20453839

2010

dbSNP: rs3731246
rs3731246
0.010 GeneticVariation BEFREE The IKZF1 SNPs, rs10235796 and rs6964969, and the CDKN2A SNP rs3731246 (previously unreported) could serve as risk markers for ALL susceptibility in Yemeni children. 28768142

2017