rs7818511, GSR

N. diseases: 1
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 paternally inherited copy of the GSR (rs7818511) A allele had a 0.31 (95%CI: 0.18, 0.53; p = 9.94 × 10<sup>-6</sup> ] risk of CTHD compared to children with the maternal copy of the same allele. 29399948 2018