Disease: Metabolic Syndrome X ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11039155
rs11039155
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
CUI: C0524620
Disease:
Metabolic Syndrome X 		0.020 GeneticVariation BEFREE Two common SNPs in NR1H3 (rs11039155 and rs2279238) and in NR1H2 (rs17373080 and rs2695121) were genotyped using TaqMan assays in MetS patients (n=265) and controls (n=219). 24100084 2013
dbSNP: rs11039155
rs11039155
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
CUI: C0524620
Disease:
Metabolic Syndrome X 		0.020 GeneticVariation BEFREE We found that the -6A allele of rs11039155 was consistently associated with a 30% reduction in risk of metabolic syndrome in the two independent population samples (adjusted OR (95% CI)=0.68 (0.53-0.86), P=0.001 for the combined sample). 18209740 2008