Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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0.040 | GeneticVariation | BEFREE | Results of the analysis provide statistically significant support for an association between the rs4132601 polymorphic site and age at diagnosis of childhood ALL (p = 0.04). | 24597983 | 2014 |
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0.040 | GeneticVariation | BEFREE | The results suggested that rs4132601 was associated with an increased ALL risk. | 25012940 | 2015 |
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0.040 | GeneticVariation | BEFREE | In addition, a borderline association was found between IKZF1 rs4132601 T>G variant and ALL risk. | 28768142 | 2017 |
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0.020 | 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 |
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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 |
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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 |
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0.040 | GeneticVariation | BEFREE | We demonstrated the association of IKZF1 polymorphism rs4132601 T/G with increased risk of ALL among Tunisian pediatric cohort, with altered phenotypic changes among ALL patients. | 31604453 | 2019 |
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0.020 | GeneticVariation | BEFREE | Two-locus (rs4132601-rs11978267) IKZF1 haplotype analysis demonstrated association of GA (P = 0.053), with increased ALL risk [OR (95% CI) = 1.58 (1.00-2.51)], which remained significant after controlling for key covariates [aP = 0.046; aOR (95% CI) = 1.61 (1.01-2.57)]. | 31604453 | 2019 |