rs1049346, GLO1

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Late onset epilepsy
CUI: C0857345
Disease: Late onset epilepsy
0.010 GeneticVariation BEFREE In particular, the rs1049346 T>C SNPs are potentially useful for risk assessment of late-onset epilepsy and DRE. 27000251 2016
Drug Resistant Epilepsy
CUI: C1096063
Disease: Drug Resistant Epilepsy
0.010 GeneticVariation BEFREE In particular, the rs1049346 T>C SNPs are potentially useful for risk assessment of late-onset epilepsy and DRE. 27000251 2016
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.010 GeneticVariation BEFREE A novel association between variant rs1049346 and ASD [OR (allele C)] = 1.5; 95 % CI = 1.1-2.2 and p < 0.05) was identified, and weak association between ASD and variant rs2736654 [OR (allele A)] = 2.2; 95 % CI = 0.99-4.9; p = 0.045) was confirmed. 24671236 2015