Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2230199
rs2230199
C3
0.900 GeneticVariation BEFREE In contrast, the C3 variants rs2230199 and rs1047286 were not associated with exudative AMD in the studied subjects. 19850835

2010
dbSNP: rs2230199
rs2230199
C3
0.900 GeneticVariation BEFREE The variant C3-rs2230199 showed no relation with AMD progression. 19797206

2010
dbSNP: rs2230199
rs2230199
C3
C 0.900 GeneticVariation GWASDB Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. 20861866

2010
dbSNP: rs2230199
rs2230199
C3
C 0.900 GeneticVariation GWASCAT Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. 20861866

2010
dbSNP: rs2230199
rs2230199
C3
C 0.900 GeneticVariation GWASCAT Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. 20385819

2010
dbSNP: rs2230199
rs2230199
C3
0.900 GeneticVariation BEFREE No interaction was found between rs2230199 and smoking or other AMD loci. 19234341

2009
dbSNP: rs2230199
rs2230199
C3
0.900 GeneticVariation BEFREE The G allele of the C3 IVS2 rs2250656, but not other tested C3 SNPs of rs2230205, rs10411506, rs2230199, rs339392, and rs163913, was significantly associated with a reduced risk for AMD in the Chinese population (OR 0.605, 95% CI 0.39-0.93, p = 0.023), even after adjusting for age, gender, smoking status, CFH rs1061170, CFB rs4151667, and CFB rs641153 allele status (OR 0.58, 95% CI 0.35-0.96, p = 0.033). 19899988

2009