rs1553368900, NRXN1

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autistic behavior
CUI: C0856975
Disease: Autistic behavior
0.700 GeneticVariation CLINVAR Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature. 23533028 2013
Autistic behavior
CUI: C0856975
Disease: Autistic behavior
0.700 GeneticVariation CLINVAR Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions. 22617343 2012