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
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