rs373413237

This variant is located in the SEMA6B gene.

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ClinVar annotation

Conflicting Classifications

2 submitters1 publication

See cases; Inborn genetic diseases

About SEMA6B

This gene encodes a member of the semaphorin family, a group of proteins characterized by the presence of a conserved semaphorin (sema) domain. Whereas some semaphorins are transmembrane proteins, others are secreted. Semaphorins play a major role in axon guidance. The protein encoded by this gene may be involved in both peripheral and central nervous system development. [provided by RefSeq, Jul 2008]

View all SEMA6B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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