MEF2D, myocyte enhancer factor 2D, 4209

N. diseases: 72; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2274316
rs2274316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.820 GeneticVariation GWASDB Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012
dbSNP: rs2274316
rs2274316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.820 GeneticVariation BEFREE Conclusion Migraine response to PACAP38 infusion in migraine without aura patients is not associated with high family load or the risk allele of rs2274316 ( MEF2D). 26994299 2017
dbSNP: rs2274316
rs2274316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.820 GeneticVariation BEFREE At one extreme, SNPs rs6790925 (near TGFBR2) and rs2274316 (MEF2D) were not associated with migraine overall, MA, or MO but were selective for migraine sub-classified by the presence of one or more of the additional migraine features. 24852292 2014
dbSNP: rs1925950
rs1925950
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.800 GeneticVariation GWASDB Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012
dbSNP: rs3790455
rs3790455
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.800 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs1050316
rs1050316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.700 GeneticVariation GWASDB Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012
dbSNP: rs10908505
rs10908505
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10908505
rs10908505
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs202206511
rs202206511
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs2274319
rs2274319
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs3790459
rs3790459
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
0.700 GeneticVariation GWASDB Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012
dbSNP: rs2274316
rs2274316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0338480
Disease:
Common Migraine
0.020 GeneticVariation BEFREE Sixteen of the patients were carriers of the risk allele rs2274316 ( MEF2D), which confers increased risk of MO and may regulate PACAP38 expression, and 16 were non-carriers. 26994298 2017
dbSNP: rs2274316
rs2274316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0338480
Disease:
Common Migraine
0.020 GeneticVariation BEFREE Conclusion Migraine response to PACAP38 infusion in migraine without aura patients is not associated with high family load or the risk allele of rs2274316 ( MEF2D). 26994299 2017
dbSNP: rs200395694
rs200395694
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE Using targeted re-sequencing of coding and conserved regulatory regions within and around 215 candidate genes selected on the basis of their known role in autoimmunity and genes associated with canine immune-mediated diseases, we identified a rare regulatory variant rs200395694:G > T located in intron 4 of the MEF2D gene encoding the myocyte-specific enhancer factor 2D transcription factor and associated with SLE in Swedish cohorts (504 SLE patients and 839 healthy controls, p = 0.014, CI = 1.1-10). 30459414 2019
dbSNP: rs200395694
rs200395694
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0004364
Disease:
Autoimmune Diseases
0.010 GeneticVariation BEFREE Using targeted re-sequencing of coding and conserved regulatory regions within and around 215 candidate genes selected on the basis of their known role in autoimmunity and genes associated with canine immune-mediated diseases, we identified a rare regulatory variant rs200395694:G > T located in intron 4 of the MEF2D gene encoding the myocyte-specific enhancer factor 2D transcription factor and associated with SLE in Swedish cohorts (504 SLE patients and 839 healthy controls, p = 0.014, CI = 1.1-10). 30459414 2019
dbSNP: rs2274316
rs2274316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0154723
Disease:
Migraine with Aura
0.010 GeneticVariation BEFREE At one extreme, SNPs rs6790925 (near TGFBR2) and rs2274316 (MEF2D) were not associated with migraine overall, MA, or MO but were selective for migraine sub-classified by the presence of one or more of the additional migraine features. 24852292 2014
dbSNP: rs2274316
rs2274316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
C 0.820 GeneticVariation GWASCAT Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs2274316
rs2274316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
C 0.820 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs3790455
rs3790455
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
C 0.800 GeneticVariation GWASDB Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012
dbSNP: rs3790455
rs3790455
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
C 0.800 GeneticVariation GWASCAT Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012
dbSNP: rs202206511
rs202206511
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
C 0.700 GeneticVariation GWASDB Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012
dbSNP: rs1925950
rs1925950
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0149931
Disease:
Migraine Disorders
G 0.800 GeneticVariation GWASCAT Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. 27322543 2016
dbSNP: rs1171563
rs1171563
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C1821417
Disease:
RESTING HEART RATE
G 0.700 GeneticVariation GWASCAT Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality. 27798624 2016
dbSNP: rs1050316
rs1050316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0018681
Disease:
Headache
T 0.700 GeneticVariation GWASCAT A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N=223,773). 29397368 2018
dbSNP: rs1050316
rs1050316
Entrez Id: 4209
Gene Symbol: MEF2D
MEF2D
CUI: C0032181
Disease:
Platelet Count measurement
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016