APOL2, apolipoprotein L2, 23780

N. diseases: 20; N. variants: 1
Disease: Alcohol Use Disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		0.010 GeneticVariation disease BEFREE The genome-wide meta-analysis of EAA in AUD revealed a significant single nucleotide polymorphism (SNP), rs916264 (p = 5.43 × 10<sup>-8</sup>), in apolipoprotein L2 (APOL2) at the genome-wide level. 31466081 2020