rs1061170, CFH

N. diseases: 72
Disease: Acute central serous chorioretinopathy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acute central serous chorioretinopathy
CUI: C0730315
Disease: Acute central serous chorioretinopathy
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms in the CFH gene were significantly associated with aCSC: rs800292 (P = 0.003, odds ratio = 1.53 [95% confidence interval = 1.15-2.03]), rs1061170 (P = 0.002, odds ratio = 0.64 [95% confidence interval = 0.48-0.86]), and rs1329428 (P = 5.87 × 10, odds ratio = 1.83 [95% confidence interval = 1.40-2.38]). 30300269 2019