rs246815

This is a intron variant variant in the SV2C gene.

GWAS Catalog Trait Associations (1)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

Parkinson disease

Allele C
OR
p 3.0e-12
N 2,525,730
Meta-analysisLarge GWAS
multi-ancestry

About SV2C

Predicted to enable transmembrane transporter activity. Predicted to be involved in several processes, including chemical synaptic transmission; neurotransmitter transport; and regulation of synaptic vesicle exocytosis. Predicted to be located in plasma membrane and synaptic vesicle. Predicted to be active in dopaminergic synapse and synaptic vesicle membrane. [provided by Alliance of Genome Resources, Apr 2025]

View all SV2C variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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