{{Rsnum
|rsid=3790455
|Gene=MEF2D
|Chromosome=1
|position=156486509
|Orientation=plus
|GMAF=0.4307
|Gene_s=MEF2D
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.7 | 48.7 | 41.6
| HCB | 9.5 | 48.2 | 42.3
| JPT | 8.0 | 37.2 | 54.9
| YRI | 63.3 | 33.3 | 3.4
| ASW | 45.6 | 43.9 | 10.5
| CHB | 9.5 | 48.2 | 42.3
| CHD | 8.3 | 47.7 | 44.0
| GIH | 8.9 | 46.5 | 44.6
| LWK | 58.2 | 33.6 | 8.2
| MEX | 24.1 | 44.8 | 31.0
| MKK | 24.4 | 53.8 | 21.8
| TSI | 9.8 | 35.3 | 54.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22683712
|Trait=None
|Title=Genome-wide association analysis identifies susceptibility loci for migraine without aura.
|RiskAllele=C
|Pval=7E-11
|OR=1.2000
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=24674449
|Title=A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}