MLXIPL, MLX interacting protein like, 51085

N. diseases: 165; N. variants: 29
Disease: Autism Spectrum Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12539160
rs12539160
Entrez Id: 51085
Gene Symbol: MLXIPL
MLXIPL
CUI: C1510586
Disease:
Autism Spectrum Disorders 		0.010 GeneticVariation BEFREE Two cases were hemizygous for the rare T allele at rs12539160 in <i>MLXIPL</i>, previously associated with ASD. 31413120 2019