rs7118648
This variant is located in the CCDC82 gene.
▶Research that mentions this SNP (1)
▶Parkinson disease loci in the mid-western AmishAssociationN=798Davis MF et al.(2013)· Human Genetics
Genome-wide association and linkage analysis in an Amish founder population (798 genotyped individuals, 31 with Parkinson disease) identified multiple susceptibility loci, with the strongest associations at chromosome 5q31.3 (MEGF10, MQLS p=5.50×10⁻⁷), chromosome 11q21 (CCDC82, p=2.16×10⁻⁷), and chromosome 15q25.1 (TMC3, p=2.31×10⁻⁷), and significant linkage evidence on chromosomes 5 (multipoint HLOD=3.77), 6 (HLOD=4.02), and 10 (HLOD=4.35). The study suggests extensive locus heterogeneity in Parkinson disease susceptibility.
About CCDC82
Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
View all CCDC82 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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