MYT1L, myelin transcription factor 1 like, 23040

N. diseases: 46; N. variants: 18
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 39 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853045
rs878853045
Entrez Id: 23040
Gene Symbol: MYT1L
MYT1L
CUI: C4225296
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 39 		T 0.700 CausalMutation CLINVAR