rs12109442, None

N. diseases: 1
Disease: Conotruncal defect ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
0.010 GeneticVariation BEFREE The risk of CTHD among children who inherited a paternally derived copy of the A allele on GLRX (rs17085159) or the T allele of GLRX (rs12109442) was 0.23 (95%CI: 0.12, 0.42; p = 1.09 × 10<sup>-6</sup> ) and 0.27 (95%CI: 0.14, 0.50; p = 2.06 × 10<sup>-5</sup> ) times the risk among children who inherited a maternal copy of the same allele. 29399948 2018