Variant: rs34927195 

    present in Gene: NLGN3
    present in Chromosome: X
    Position on Chromosome: 71147958
    Alleles of this Variant: -/G

rs34927195 in NLGN3 gene and Dysmorphic features PMID 23849776 2013 Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.

PMID 15150161 2004 Disorder-associated mutations lead to functional inactivation of neuroligins.

PMID 24570023 2014 Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.

PMID 12669065 2003 Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.

rs34927195 in NLGN3 gene and Overgrowth PMID 23849776 2013 Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.

PMID 12669065 2003 Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.

PMID 24570023 2014 Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.

PMID 15150161 2004 Disorder-associated mutations lead to functional inactivation of neuroligins.