CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE In our patients, p.I62V, but not p.Y402H, was significantly associated with an increased risk of AMD. 29367644 2018
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE To pool the results of published data regarding association of ARMS2/LOC387715 A69S, CFH Y402H and CFH I62V genotypes with age-related macular degeneration (AMD) with and without reticular pseudodrusen (RPD). 28593728 2018
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Blood samples from all subjects were genotyped for major age-related macular degeneration (AMD)-associated single nucleotide polymorphisms (SNPs) the major AMD-associated SNPs; CFH Y402H rs1061170, CFH I62V rs800292, ARMS2 A69S rs10490924. 30596689 2018
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE We have previously shown a strong association of C3 (R102G) and CFH Y402H with AMD whereas no association was found for CCL2-2518. 28095095 2017
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Exploratory analyses observed that the association between xanthophyll intake and AMD varied statistically significantly by CFH rs1061170 genotype among Caucasians (p for interaction = 0.045) but not African Americans. 28332910 2017
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Pooled overall odds ratios for RAP/AMD were 1.15 (95% CI 0.60-2.18) for GT versus GG, 3.52 (95% CI 1.25-9.91) for TT versus GG ARMS2, 0.98 (95% CI 0.22-4.29) for GA versus AA, 1.00 (95% CI 0.25-4.02) for GG versus AA CFHI62V, 0.57 (95% CI 0.35-0.93) for CT versus TT CFH Y402H, and 0.40 (95% CI 0.22-0.74) for CC versus TT CFH Y402H. 28005184 2017
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE However, higher levels of CRP in the presence of C allele of Y402H might confer more risk for the development of exudative AMD. 27778189 2017
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Two variants in the complement factor H (CFH) gene, Y402H and I62V, are strongly associated with risk of AMD. 27647805 2017
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Complement factor H polymorphism in exon 9 (Y402H) has shown a strong association with susceptibility to AMD resulting in complement activation, recruitment of phagocytes, RPE damage, and visual decline. 28913923 2017
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
G 0.900 GeneticVariation GWASCAT We confirmed the association of age-related maculopathy susceptibility 2 (ARMS2) rs10490924 (P=7.38 × 10<sup>-17</sup>), HTRA1 rs11200638 (P=5.47 × 10<sup>-17</sup>) and complement factor H gene (CFH) rs800292 (P=2.53 × 10<sup>-8</sup>) with neovascular AMD, all loci passing the genome-wide significance level (P<5.22 × 10<sup>-8</sup>). 28703135 2017
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Association of ARMS2/LOC387715 A69S, CFH Y402H, and CFH I62V polymorphisms with retinal angiomatous proliferation compared with typical age-related macular degeneration: a meta-analysis. 28005184 2017
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE We confirmed the association of age-related maculopathy susceptibility 2 (ARMS2) rs10490924 (P=7.38 × 10<sup>-17</sup>), HTRA1 rs11200638 (P=5.47 × 10<sup>-17</sup>) and complement factor H gene (CFH) rs800292 (P=2.53 × 10<sup>-8</sup>) with neovascular AMD, all loci passing the genome-wide significance level (P<5.22 × 10<sup>-8</sup>). 28703135 2017
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Two variants in the complement factor H (CFH) gene, Y402H and I62V, are strongly associated with risk of AMD. 27647805 2017
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE CFH Y402H SNP might be protective for AMD in the Turkish population. 27404493 2016
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE The polymorphism rs1061170/Y402H might be a genetic predictor of treatment response to anti-VEGF therapy in AMD patients. 27151934 2016
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Odds ratios, especially for the main risk polymorphisms in ARMS2 (rs10490924) and CFH (rs1061170), gained with increasing disease severity and bilateralism (exemplarily: rs1061170: unilateral early AMD: OR = 1.18; bilateral early AMD: OR = 1.20; unilateral intermediate AMD: OR = 1.28; bilateral intermediate AMD: OR = 1.39, unilateral geographic atrophy (GA): OR = 1.50; bilateral GA: OR = 1.71). 27257685 2016
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Association of Combined Complement Factor H Y402H and ARMS/LOC387715 A69S Polymorphisms with Age-related Macular Degeneration: A Meta-analysis. 27269047 2016
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE To evaluate the association of extramacular drusen (EMD) with age-related macular degeneration (AMD) and with complement factor H (CFH rs1061170) and age-related maculopathy susceptibility 2 (ARMS2 rs10490924) polymorphisms in individuals with and without AMD. 26614632 2016
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Based on this, we conclude that liver-kidney yin-deficiency AMD is associated with the C allele and TC and CC genotypes of the CFH Y402H polymorphism. 27706724 2016
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE AMD individuals who had at least one copy of the C allele of rs1061170 had an increased risk of disease compared with cases with the T allele. 25612476 2016
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE AG genotype of CCL2-2518 in combination with TT genotype of CFH Y402H showed significant protective effect against AMD. 27316788 2016
dbSNP: rs1061170
rs1061170
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE This meta-analysis suggested that CFH rs1061170 and rs1410996 polymorphisms were associated with AMD risk, both of which demonstrated a higher susceptibility to AMD, especially to nAMD. 26727378 2016
dbSNP: rs1410996
rs1410996
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE This meta-analysis suggested that CFH rs1061170 and rs1410996 polymorphisms were associated with AMD risk, both of which demonstrated a higher susceptibility to AMD, especially to nAMD. 26727378 2016
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Rs12153855C and rs9391734A alleles could further increase the susceptibility to AMD in subjects with rs800292, rs11200638 and rs429608 risk alleles. 26861912 2016
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease:
Age related macular degeneration
0.900 GeneticVariation BEFREE Patients were genotyped to identify major single nucleotide polymorphisms associated with AMD (CFH Y402, CFH I62V, and ARMS2 A69S). 27521170 2016