CD36, CD36 molecule, 948

N. diseases: 351; N. variants: 61
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3211938
rs3211938
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs3211938
rs3211938
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.800 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs3211938
rs3211938
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.800 GeneticVariation GWASDB Initial discovery and in silico follow-up in 7,000 additional African American samples, confirmed two novel loci: rs5030359 within ICAM1 is associated with total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-C) (p = 8.8×10(-7) and p = 1.5×10(-6) respectively) and a nonsense mutation rs3211938 within CD36 is associated with high-density lipoprotein cholesterol (HDL-C) levels (p = 13.5×10(-12)). 23236364 2012
dbSNP: rs3211938
rs3211938
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.800 GeneticVariation GWASDB Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project. 22629316 2012
dbSNP: rs121918035
rs121918035
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		0.800 GeneticVariation UNIPROT Identification of cryptic splice site, exon skipping, and novel point mutations in type I CD36 deficiency. 11950861 2002
dbSNP: rs142186404
rs142186404
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		0.800 GeneticVariation UNIPROT Identification of cryptic splice site, exon skipping, and novel point mutations in type I CD36 deficiency. 11950861 2002
dbSNP: rs75326924
rs75326924
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		0.800 GeneticVariation UNIPROT Identification of cryptic splice site, exon skipping, and novel point mutations in type I CD36 deficiency. 11950861 2002
dbSNP: rs75326924
rs75326924
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		T 0.800 CausalMutation CLINVAR Identification of cryptic splice site, exon skipping, and novel point mutations in type I CD36 deficiency. 11950861 2002
dbSNP: rs75326924
rs75326924
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		T 0.800 CausalMutation CLINVAR Human CD36 deficiency is associated with elevation in low-density lipoprotein-cholesterol. 10946357 2000
dbSNP: rs75326924
rs75326924
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		T 0.800 CausalMutation CLINVAR Phenotype-genotype correlation in CD36 deficiency types I and II. 11019968 2000
dbSNP: rs121918035
rs121918035
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		0.800 GeneticVariation UNIPROT Molecular basis of CD36 deficiency. Evidence that a 478C-->T substitution (proline90-->serine) in CD36 cDNA accounts for CD36 deficiency. 7533783 1995
dbSNP: rs142186404
rs142186404
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		0.800 GeneticVariation UNIPROT Molecular basis of CD36 deficiency. Evidence that a 478C-->T substitution (proline90-->serine) in CD36 cDNA accounts for CD36 deficiency. 7533783 1995
dbSNP: rs75326924
rs75326924
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		0.800 GeneticVariation UNIPROT Molecular basis of CD36 deficiency. Evidence that a 478C-->T substitution (proline90-->serine) in CD36 cDNA accounts for CD36 deficiency. 7533783 1995
dbSNP: rs75326924
rs75326924
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		T 0.800 CausalMutation CLINVAR Molecular basis of CD36 deficiency. Evidence that a 478C-->T substitution (proline90-->serine) in CD36 cDNA accounts for CD36 deficiency. 7533783 1995
dbSNP: rs75326924
rs75326924
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		T 0.800 CausalMutation CLINVAR A novel polymorphism in glycoprotein IV (replacement of proline-90 by serine) predominates in subjects with platelet GPIV deficiency. 7686693 1993
dbSNP: rs121918035
rs121918035
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		C 0.800 CausalMutation CLINVAR
dbSNP: rs142186404
rs142186404
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1842090
Disease:
Platelet Glycoprotein IV Deficiency 		C 0.800 CausalMutation CLINVAR
dbSNP: rs13236689
rs13236689
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0032181
Disease:
Platelet Count measurement 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs2366855
rs2366855
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3173805
rs3173805
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3211931
rs3211931
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7755
rs7755
Entrez Id: 948
Gene Symbol: CD36
CD36
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: rs7755
rs7755
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11974777
rs11974777
Entrez Id: 948
Gene Symbol: CD36
CD36
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: rs139761834
rs139761834
Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0032181
Disease:
Platelet Count measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018