MED13L, mediator complex subunit 13L, 23389

N. diseases: 94; N. variants: 49
Disease: Attention deficit hyperactivity disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555247672
rs1555247672
Entrez Id: 23389
Gene Symbol: MED13L
MED13L
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		A 0.700 CausalMutation CLINVAR