Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs671
rs671
Entrez Id: 217
Gene Symbol: ALDH2
ALDH2
CUI: C0201899
Disease:
Aspartate aminotransferase measurement
A 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