Disease: Coronary heart disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.020 GeneticVariation disease BEFREE Considering that the rs2119289 of FIGN gene is related to the appropriate folate level, FIGN might play an important role in CHD by upregulating plasma folate concentration during embryo heart development. 28534241 2017
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.020 GeneticVariation disease BEFREE The +94762G>C (rs2119289) variant in intron 4 of the <i>FIGN</i> gene was associated with significant reduction in CHD susceptibility (<i>P</i>=5.1×10<sup>-14</sup> for the allele, <i>P</i>=8.5×10<sup>--13</sup> for the genotype). 28302752 2017