rs61754480

This variant is located in the SCFD1 gene.

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ClinVar annotation

Uncertain Significance★★★☆

3 submitters1 publication

Amyotrophic lateral sclerosis; SCFD1-related disorder; not provided

About SCFD1

Predicted to enable syntaxin binding activity. Involved in negative regulation of autophagosome assembly; regulation of protein transport; and response to toxic substance. Located in cis-Golgi network. [provided by Alliance of Genome Resources, Jul 2025]

View all SCFD1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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