Varaico: Literature-Extracted Genetic Variants

Gene:KCNK18
Variant:p.F139fs
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KCNK18

NM_181840.1:p.F139fs

Associated Papers

Opportunistic genomic screening has clinical utility: An interventional cohort study.

Mighton C et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2025

Case Report: Decoding genetic risks of vascular parkinsonism: a case series.

Shalash A et al.

Frontiers in Genetics, 2025

Genetics of migraine: complexity, implications, and potential clinical applications.

Sutherland HG et al.

The Lancet. Neurology, 2024

Genetics of migraine: where are we now?

Grangeon L et al.

The Journal of Headache and Pain, 2023

Study of variants in genes implicated in rare familial migraine syndromes and their association with migraine in 200,000 exome-sequenced UK Biobank participants.

Markel KA et al.

Annals of Human Genetics, 2022

Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic Neuropathy.

Ślęczkowska M et al.

International Journal of Molecular Sciences, 2022

Workflow for the Implementation of Precision Genomics in Healthcare.

Mehandziska S et al.

Frontiers in Genetics, 2020

32695137 (PubMed )
Supplement: Data_Sheet_2.XLSX › Rare_diseases
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."