MEF2C, myocyte enhancer factor 2C, 4208

N. diseases: 206; N. variants: 53
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4521516
rs4521516
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		G 0.800 GeneticVariation GWASCAT New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
dbSNP: rs4521516
rs4521516
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		G 0.800 GeneticVariation GWASDB New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
dbSNP: rs700585
rs700585
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0032181
Disease:
Platelet Count measurement 		C 0.800 GeneticVariation GWASCAT New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
dbSNP: rs700585
rs700585
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0032181
Disease:
Platelet Count measurement 		C 0.800 GeneticVariation GWASDB New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
dbSNP: rs10514303
rs10514303
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs1065861
rs1065861
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs1422189
rs1422189
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs1561824498
rs1561824498
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C1510586
Disease:
Autism Spectrum Disorders 		A 0.700 CausalMutation CLINVAR Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. 30763456 2019
dbSNP: rs186783371
rs186783371
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C4048548
Disease:
Anti-Mullerian Hormone Measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of anti-Müllerian hormone levels in pre-menopausal women of late reproductive age and relationship with genetic determinants of reproductive lifespan. 30649302 2019
dbSNP: rs2067663
rs2067663
Entrez Id: 4208;101929423
Gene Symbol: MEF2C;MEF2C-AS1
MEF2C;MEF2C-AS1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2067663
rs2067663
Entrez Id: 4208;101929423
Gene Symbol: MEF2C;MEF2C-AS1
MEF2C;MEF2C-AS1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3850651
rs3850651
Entrez Id: 4208;101929423
Gene Symbol: MEF2C;MEF2C-AS1
MEF2C;MEF2C-AS1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs41352752
rs41352752
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs61104616
rs61104616
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs62380364
rs62380364
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs796052733
rs796052733
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C1510586
Disease:
Autism Spectrum Disorders 		A 0.700 CausalMutation CLINVAR Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. 30763456 2019
dbSNP: rs10066711
rs10066711
Entrez Id: 4208;101929423
Gene Symbol: MEF2C;MEF2C-AS1
MEF2C;MEF2C-AS1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs10514303
rs10514303
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs17551090
rs17551090
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C4049938
Disease:
Physical Activity Measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE. 29899525 2018
dbSNP: rs3047819
rs3047819
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		T 0.700 GeneticVariation GWASCAT A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. 29325848 2018
dbSNP: rs34316
rs34316
Entrez Id: 4208;109729137
Gene Symbol: MEF2C;MEF2C-AS2
MEF2C;MEF2C-AS2
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs606393
rs606393
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs61104616
rs61104616
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs61104616
rs61104616
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs770463
rs770463
Entrez Id: 4208;101929423
Gene Symbol: MEF2C;MEF2C-AS1
MEF2C;MEF2C-AS1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018