rs671, ALDH2

N. diseases: 116
Disease: Aspartate aminotransferase measurement ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Aspartate aminotransferase measurement
CUI: C0201899
Disease: Aspartate aminotransferase measurement
0.700 GeneticVariation GWASCAT Moreover, 9 missense variants were newly identified, of which we identified new associations between a common population-specific missense variant, rs671 (p.Glu457Lys) of ALDH2, and two traits including aspartate aminotransferase (P = 5.20 × 10<sup>-13</sup>) and alanine aminotransferase (P = 4.98 × 10<sup>-8</sup>). 30718733 2019