Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9619
Gene Symbol: ABCG1
ABCG1
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
Polypoidal choroidal vasculopathy 		0.030 GeneticVariation BEFREE We found that in Asian population, CETP rs3764261 (T allele; OR = 1.46; 95% CI: 1.28-1.665, <i>P</i> < 0.01), CETP rs2303790 (G allele; OR = 1.57; 95% CI: 1.258-1.96, <i>P</i> < 0.01), and ABCG1 rs57137919 (A allele; OR = 1.168; 95% CI: 1.016-1.343, <i>P</i> < 0.01) were significantly associated with PCV, and ABCG1 rs57137919 (A allele; OR = 1.208, 95% CI: 1.035-1.411, <i>P</i> < 0.01) has different effects in PCV and AMD. 29977615

2018
Entrez Id: 9619
Gene Symbol: ABCG1
ABCG1
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
Polypoidal choroidal vasculopathy 		0.030 GeneticVariation BEFREE In this study, we have newly identified a haplotype-tagging SNP, rs225396, in ABCG1 to be associated with PCV and nAMD in Chinese and Japanese cohorts. 27787563

2016
Entrez Id: 9619
Gene Symbol: ABCG1
ABCG1
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
Polypoidal choroidal vasculopathy 		0.030 GeneticVariation BEFREE A borderline association was detected between the ATP-binding cassette, subfamily G, member 1 (ABCG1) gene SNP rs57137919 and PCV (P = 0.03). 24393350

2014