13q21, 16p13, 17q21.31, 21q21.3, 4q13, 4q21, 8q13, AKT, AKT serine/threonine kinase 1, ARL17A, BLK, BTC, CCDC94, EGFR, ENST00000547372, ENST00000547372;, ERK, ET, ET candidate genes, ETS2, EYA1, Essential tremor, G, MAPT, N6AMT1, NPY4R, PCDH9, PDPR, PI3K, PZP, RBFOX1, RNA, SCARB2, SPATA21, SPINK5, STEAP1B, TBC1D3C, TUBB2A, VPS33B, WGS, ZNF736, ZRANB1, bilateral kinetic tremor of the arms, c.4-2A, cancer, candidate genes, chromosome 16p13, collapsed, epidermal growth factor receptor-phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha, essential tremor, exon 2, familial essential tremor, gamma-aminobutyric acid, gene regions, haplotype, neurological disease, neurological disorders, oxygen, patients, phosphatidylinositol-4,5-bisphosphate, protein Kinase 1, rare variants, serine, threonine, tremor