MED13L, mediator complex subunit 13L, 23389

N. diseases: 94; N. variants: 49
Disease: Moderate intellectual disability ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312707
rs869312707
Entrez Id: 23389
Gene Symbol: MED13L
MED13L
CUI: C0026351
Disease:
Moderate intellectual disability 		A 0.700 CausalMutation CLINVAR
dbSNP: rs869312875
rs869312875
Entrez Id: 23389
Gene Symbol: MED13L
MED13L
CUI: C0026351
Disease:
Moderate intellectual disability 		TC 0.700 CausalMutation CLINVAR