Gene entry

SPPL2C

signal peptide peptidase like 2C

Chromosome: 17
Cytoband: 17q21.31
Variants (rsID): 3

SPPL2C 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 “signal peptide peptidase like 2C”. The reference table lists 3 variants (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs12185268Not classifiedmissense_variantMultiple System Atrophy 1|Parkinson Disease, Late-Onset|Rem Sleep Behavior Disorder|Fainting|Autonomic Dysfunction|Head Injury

Other listed variants

rs242944
rs929223

Public references

NCBI Gene
Ensembl
ClinVar

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