Variant: rs369100678 

    present in Gene: VPS13C
    present in Chromosome: 15
    Position on Chromosome: 61958608
    Alleles of this Variant: C/G

rs369100678 in VPS13C gene and PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET PMID 26942284 2016 Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

rs369100678 in VPS13C gene and Parkinson Disease PMID 26942284 2016 Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.