rs10109552 - NAT2 - PSD3

Magnitude 2.8 · 1 study on file

Reported associations

  • Genome-wide association study in essential tremor identifies three new loci - Unknown journal (n.d.) · Unknown authors · PubMed 27797806

    ABSTRACT: Essential tremor has a high heritability, but its molecular genetic determinants remain unknown. Müller et al. conduct a genome-wide association study in more than 2800 patients with essential tremor and more than 6800 controls of European descent, and identify three new loci associated with the disease. We conducted a genome-wide association study of essential tremor, a common movement disorder characterized mainly by a postural and kinetic tremor of the upper extremities. Twin and family history studies show a high heritability for essential tremor. The molecular genetic determinants of essential tremor are unknown. We included 2807 patients and 6441 controls of European descent in our two-stage genome-wide association study. The 59 most significantly disease-associated marker


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Lifestyle context

Concrete actions anchored to the cited research. We do not prescribe, we describe.

Screening

  • essential tremor screening Moderate

    Genetic variant associated with increased essential tremor risk (GWAS p=2.00e-8, n=7154, OR=1.235)

    Discuss tremor risk with healthcare provider; report any new hand, head, or voice tremor