rs760449914

This variant is located in the NLGN1 gene.

ClinVar annotation

Uncertain Significance☆☆☆
1 submitter

Inborn genetic diseases

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About NLGN1

This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. [provided by RefSeq, Jul 2008]

View all NLGN1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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