MEF2C, myocyte enhancer factor 2C, 4208

N. diseases: 206; N. variants: 53
Disease: Aphasia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1085307051
rs1085307051
Entrez Id: 4208;101929423
Gene Symbol: MEF2C;MEF2C-AS1
MEF2C;MEF2C-AS1
CUI: C0003537
Disease:
Aphasia 		G 0.700 GeneticVariation CLINVAR