rs2274316, MEF2D

N. diseases: 3
Disease: Migraine Disorders ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Migraine Disorders
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
Migraine Disorders
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
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
0.820 GeneticVariation GWASCAT Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
0.820 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
0.820 GeneticVariation GWASDB Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012