rs2477700016

This variant is located in the SEMA5A gene.

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ClinVar annotation

Uncertain Significance

1 submitter

SEMA5A-related disorder

About SEMA5A

This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Members of this family are involved in axonal guidance during neural development. This gene has been implicated as an autism susceptibility gene.[provided by RefSeq, Jan 2010]

View all SEMA5A variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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