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Gene entry

NSF

N-ethylmaleimide sensitive factor, vesicle fusing ATPase

Chromosome
17
Cytoband
17q21.31
Variants (rsID)
6

NSF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q21.31). Its official name is “N-ethylmaleimide sensitive factor, vesicle fusing ATPase”. The reference table lists 6 variants (rsID) for this gene.

Clinically classified variants

1 reference-table entries with clinical significance.

  • rs199533Not classifiedsynonymous_variantAlzheimer Disease

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.