CD33, CD33 molecule, 945

N. diseases: 142; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3865444
rs3865444
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0002395
Disease:
Alzheimer's Disease 		A 0.900 GeneticVariation GWASCAT Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. 30617256 2019
dbSNP: rs3865444
rs3865444
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0002395
Disease:
Alzheimer's Disease 		0.900 GeneticVariation GWASCAT Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. 21460841 2011
dbSNP: rs12459419
rs12459419
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12459419
rs12459419
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs12459419
rs12459419
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12459419
rs12459419
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1354106
rs1354106
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs201074739
rs201074739
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs2455069
rs2455069
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0202236
Disease:
Triglycerides measurement 		G 0.700 GeneticVariation GWASCAT Genetic architecture of human plasma lipidome and its link to cardiovascular disease. 31551469 2019
dbSNP: rs3865444
rs3865444
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0023508
Disease:
White Blood Cell Count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3865444
rs3865444
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0032181
Disease:
Platelet Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3865444
rs3865444
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3865444
rs3865444
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0002395
Disease:
Alzheimer's Disease 		0.900 GeneticVariation GWASDB Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. 21460841 2011
dbSNP: rs3865444
rs3865444
Entrez Id: 945
Gene Symbol: CD33
CD33
CUI: C0162534
Disease:
Prion Diseases 		0.700 GeneticVariation GWASDB Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. 22210626 2012