VPS13C Chromosome 15

Vacuolar protein sorting 13 homolog C
83 variants 83 Health Risk

Upload your DNA to see your personal genotypes for variants in VPS13C.

What This Gene Does
Involved in mitochondrion organization and negative regulation of type 2 mitophagy. Located in several cellular components, including late endosome; lipid droplet; and mitochondrial outer membrane. Implicated in Parkinson's disease 23. [provided by Alliance of Genome Resources, Jul 2025]
Gene Info
Gene Group
Bridge-like lipid transfer protein family
Locus Type
gene with protein product
Location
15q22.2
Ensembl
ENSG00000129003
Associated Conditions (6)
Autosomal recessive early-onset Parkinson disease 23
Inborn genetic diseases
VPS13C-related disorder
Young-onset Parkinson disease
Gastric cancer
Parkinson disease
Key Variants
All Variants (83)
RSID Category Clinical Significance Conditions
RS2045915658 Health Risk Pathogenic —
RS2140069494 Health Risk Pathogenic —
RS2140234163 Health Risk Pathogenic Autosomal recessive early-onset Parkinson disease 23, Autosomal recessive early-onset Parkinson disease 23
RS2140329273 Health Risk Pathogenic —
RS2541910203 Health Risk Pathogenic —
RS2547818083 Health Risk Pathogenic —
RS2547886688 Health Risk Pathogenic —
RS2547891117 Health Risk Pathogenic —
RS2547893982 Health Risk Pathogenic —
RS2548147835 Health Risk Pathogenic —
RS527383658 Health Risk Pathogenic —
RS571944290 Health Risk Pathogenic —
RS751054856 Health Risk Pathogenic —
RS757630901 Health Risk Pathogenic —
RS761323769 Health Risk Pathogenic —
RS767007361 Health Risk Pathogenic —
RS767990486 Health Risk Pathogenic —
RS775841187 Health Risk Pathogenic —
RS778239562 Health Risk Pathogenic —
RS779017939 Health Risk Pathogenic —
RS869312809 Health Risk Pathogenic Autosomal recessive early-onset Parkinson disease 23, Parkinson disease, Autosomal recessive early-onset Parkinson disease 23
RS869312810 Health Risk Pathogenic Autosomal recessive early-onset Parkinson disease 23, Parkinson disease, Autosomal recessive early-onset Parkinson disease 23
RS869312811 Health Risk Pathogenic Autosomal recessive early-onset Parkinson disease 23, Parkinson disease, Autosomal recessive early-onset Parkinson disease 23
RS869320761 Health Risk Pathogenic Autosomal recessive early-onset Parkinson disease 23, Autosomal recessive early-onset Parkinson disease 23
RS879253853 Health Risk Pathogenic Parkinson disease, Parkinson disease
RS916946765 Health Risk Pathogenic —
RS1315150327 Health Risk Pathogenic/Likely pathogenic —
RS138846118 Health Risk Pathogenic/Likely pathogenic Autosomal recessive early-onset Parkinson disease 23, Autosomal recessive early-onset Parkinson disease 23
RS148074630 Health Risk Pathogenic/Likely pathogenic Autosomal recessive early-onset Parkinson disease 23, Autosomal recessive early-onset Parkinson disease 23
RS369100678 Health Risk Pathogenic/Likely pathogenic Autosomal recessive early-onset Parkinson disease 23, Parkinson disease, Young-onset Parkinson disease
RS752457309 Health Risk Pathogenic/Likely pathogenic Autosomal recessive early-onset Parkinson disease 23, Young-onset Parkinson disease, Autosomal recessive early-onset Parkinson disease 23
RS755656180 Health Risk Pathogenic/Likely pathogenic Autosomal recessive early-onset Parkinson disease 23, Autosomal recessive early-onset Parkinson disease 23
RS756149444 Health Risk Pathogenic/Likely pathogenic —
Sign Up to Analyze Your DNA Log In