rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
0.840
GeneticVariation
BEFREE
Con-clusion: CFI rs10033900 and rs2285714 polymorphisms in a Turkish population were not associated with AMD .
31614353
2019
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
0.840
GeneticVariation
BEFREE
To determine the impact of <i>HTRA1</i> rs1120638, <i>TIMP3</i> rs9621532, <i>VEGFA</i> rs833068, <i>CFI</i> rs10033900 , <i>ERCC6</i> rs3793784, and <i>KCTD10</i> rs56209061 genotypes on the development of age-related macular degeneration (AMD) in the Lithuanian population.
31583032
2019
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
0.840
GeneticVariation
GWASCAT
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
26691988
2016
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
T
0.840
GeneticVariation
GWASDB
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.
22705344
2012
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
T
0.840
GeneticVariation
GWASDB
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
21665990
2011
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
T
0.840
GeneticVariation
GWASCAT
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
21665990
2011
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
0.840
GeneticVariation
BEFREE
Individuals with the homozygous CFI rs10033900 TT genotype had a 2.9 [1.2-7.2]-fold increased risk, and those with the CFH Y402H GG genotype had a 2.2 [1.0-4.8]-fold higher risk of developing AMD compared with non-carriers.
21906714
2011
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
0.840
GeneticVariation
GWASCAT
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).
20385826
2010
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
0.840
GeneticVariation
BEFREE
There was a possible association between LIPC and complement factor H (CFH) rs1410996, and a possible interaction effect between LIPC and both CFH rs10033900 and the complement factor I (CFI) variants in terms of risk of AMD .
21139980
2010
rs10033900
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
Age related macular degeneration
0.840
GeneticVariation
GWASDB
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).
20385826
2010
rs121964914
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.
19821824
2010
rs121964914
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
20513133
2010
rs121964917
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
20513133
2010
rs121964917
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.
19821824
2010
rs121964918
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.
19821824
2010
rs121964918
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
20513133
2010
rs121964914
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Atypical hemolytic-uremic syndrome.
19846853
2009
rs121964917
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Atypical hemolytic-uremic syndrome.
19846853
2009
rs121964918
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Atypical hemolytic-uremic syndrome.
19846853
2009
rs121964914
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome.
17106690
2007
rs121964917
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome.
17106690
2007
rs121964918
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome.
17106690
2007
rs121964914
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome.
16621965
2006
rs121964917
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome.
16621965
2006
rs121964918
×
Entrez Id:
3426
Gene Symbol:
CFI
CFI
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3
0.800
GeneticVariation
UNIPROT
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome.
16621965
2006