C9, complement C9, 735

N. diseases: 62; N. variants: 32
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34882957
rs34882957
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C3810042
Disease:
MACULAR DEGENERATION, AGE-RELATED, 15 		0.800 GeneticVariation UNIPROT Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration. 24036952 2013
dbSNP: rs121909593
rs121909593
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C3151189
Disease:
C9 Deficiency 		0.800 GeneticVariation UNIPROT Heterogeneity in the genetic basis of human complement C9 deficiency. 9634479 1998
dbSNP: rs121909593
rs121909593
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C3151189
Disease:
C9 Deficiency 		C 0.800 CausalMutation CLINVAR
dbSNP: rs34882957
rs34882957
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C3810042
Disease:
MACULAR DEGENERATION, AGE-RELATED, 15 		A 0.800 SusceptibilityMutation CLINVAR
dbSNP: rs10062079
rs10062079
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		A 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
dbSNP: rs11951093
rs11951093
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs11951093
rs11951093
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs11959928
rs11959928
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs12153248
rs12153248
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. 30604766 2019
dbSNP: rs1362800
rs1362800
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0022661
Disease:
Kidney Failure, Chronic 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs1362800
rs1362800
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs138107037
rs138107037
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs1818782
rs1818782
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1818782
rs1818782
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0005612
Disease:
Birth Weight 		C 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs2542713
rs2542713
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs2542713
rs2542713
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0011847
Disease:
Diabetes 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs2542713
rs2542713
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0011849
Disease:
Diabetes Mellitus 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs34356831
rs34356831
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs1818782
rs1818782
Entrez Id: 735;1601
Gene Symbol: C9;DAB2
C9;DAB2
CUI: C0201899
Disease:
Aspartate aminotransferase measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs265721
rs265721
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs62358361
rs62358361
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs62358364
rs62358364
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs835209
rs835209
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs10064820
rs10064820
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11953280
rs11953280
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017