rs16944558, COLEC12

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.710 GeneticVariation BEFREE Our data showed an association of MetS at the genome-wide significance level (<i>P</i> < 8.6 x 10<sup>-8</sup>) with two SNPs, including the rs662799 SNP in the apolipoprotein A5 (<i>APOA5</i>) gene and the rs16944558 SNP in the collectin subfamily member 12 (<i>COLEC12</i>) gene. 29212154 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.710 GeneticVariation GWASCAT Additionally, we found that an interaction between the <i>APOA5</i> rs662799 and <i>COLEC12</i> rs16944558 SNPs influenced MetS, high triglyceride, and low HDL. 29212154 2017