XRCC1, X-ray repair cross complementing 1, 7515

N. diseases: 410; N. variants: 39
Disease: Myocardial Infarction ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.030 GeneticVariation disease BEFREE For the other two NEIL3 SNPs (rs10013040 and rs1395479) and for the SNPs of OGG1 (rs1052133), APEX1 (rs1878703) and XRCC1 (rs25489) we observed no association with risk of myocardial infarction. 25703835 2015
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.030 GeneticVariation disease BEFREE There appeared to be a significant difference in the distribution of genotype and allele frequencies of XRCC1 Arg399Gln polymorphism between T2DM groups with and without CAD (p=0.03), albeit no significant association with MI was observed (p=0.055). 23360319 2013
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.030 GeneticVariation disease LHGDN APE1 and XRCC3 polymorphisms and myocardial infarction. 18712175 2008