NLGN4X, neuroligin 4 X-linked, 57502

N. diseases: 6; N. variants: 6
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12009217
rs12009217
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. 29483656 2018
dbSNP: rs12845396
rs12845396
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Biological insights from 108 schizophrenia-associated genetic loci. 25056061 2014
dbSNP: rs1569118680
rs1569118680
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C1845539
Disease:
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		G 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1569118680
rs1569118680
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C3501611
Disease:
Mental Retardation, X-Linked Nonsyndromic 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1569118853
rs1569118853
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C1845334
Disease:
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		CA 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1569118853
rs1569118853
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C1845539
Disease:
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		CA 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs749477993
rs749477993
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs756651509
rs756651509
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C1845539
Disease:
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		A 0.700 CausalMutation CLINVAR