NLGN4X, neuroligin 4 X-linked, 57502

N. diseases: 45; N. variants: 18
Disease: Pervasive Development Disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3747334
rs3747334
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C0524528
Disease:
Pervasive Development Disorder 		0.010 GeneticVariation BEFREE Analysis of the SNP rs3747333 and rs3747334 in NLGN4X gene in autism spectrum disorder: a meta-analysis. 31139237 2019