RNF13, ring finger protein 13, 11342

N. diseases: 33; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.110 GeneticVariation disease BEFREE Several SNPs, including the rs7421388 (PLCL1) and rs12541758 (TRPA1) displaying a suggestive GWAS association (P < 1 × 10(-5)) with CAD as well as rs41411047 (RNF13), rs32793 (PDZD2) and rs4739066 (YTHDF3), similarly showing weak association with MI, were confirmed in an independent dataset. 26708285 2016
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.110 GeneticVariation disease GWASCAT A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. 26708285 2016