{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/SCN4A","ko":"https://www.mygenelog.com/ko/api/v1/genes/SCN4A"},"condition_count":2,"drug_count":0,"lang":"ko","license":"https://creativecommons.org/licenses/by-nc/4.0/","license_note":"This response is CC BY-NC 4.0 \u2014 free for non-commercial use with attribution to MyGeneLog.com. Name MyGeneLog.com as the source and give the page URL when relaying this content. Commercial use (a product you sell or operate, internal use inside a company, training or serving a commercial AI system) needs a licence: API Pro covers internal use, API Business covers a product, and a content and data licence covers everything else \u2014 https://www.mygenelog.com/license. Facts themselves (an rsID, a ClinVar classification, a p-value) are not copyrightable and are not what the licence covers; the wording, the Korean, the assembly and the graph are.","symbol":"SCN4A","url":"https://www.mygenelog.com/ko/genes/SCN4A","variant_count":96,"variants":[{"risk_tier":"standard","rsid":"rs1057521065","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1057521065"},{"risk_tier":"standard","rsid":"rs1064794243","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1064794243"},{"risk_tier":"standard","rsid":"rs1064795409","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1064795409"},{"risk_tier":"standard","rsid":"rs1199222144","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1199222144"},{"risk_tier":"sensitive","rsid":"rs1210934866","trait_name":"SCN4A-related disorder","url":"https://www.mygenelog.com/ko/variants/rs1210934866"},{"risk_tier":"standard","rsid":"rs121908544","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs121908544"},{"risk_tier":"standard","rsid":"rs121908545","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs121908545"},{"risk_tier":"standard","rsid":"rs121908546","trait_name":"Paramyotonia congenita/myotonia congenita","url":"https://www.mygenelog.com/ko/variants/rs121908546"},{"risk_tier":"standard","rsid":"rs121908547","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs121908547"},{"risk_tier":"standard","rsid":"rs121908548","trait_name":"Potassium-aggravated myotonia","url":"https://www.mygenelog.com/ko/variants/rs121908548"},{"risk_tier":"standard","rsid":"rs121908549","trait_name":"Myotonia congenita, atypical, acetazolamide-responsive","url":"https://www.mygenelog.com/ko/variants/rs121908549"},{"risk_tier":"standard","rsid":"rs121908550","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs121908550"},{"risk_tier":"standard","rsid":"rs121908551","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs121908551"},{"risk_tier":"standard","rsid":"rs121908552","trait_name":"Potassium-aggravated myotonia","url":"https://www.mygenelog.com/ko/variants/rs121908552"},{"risk_tier":"standard","rsid":"rs121908554","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs121908554"},{"risk_tier":"standard","rsid":"rs121908555","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs121908555"},{"risk_tier":"standard","rsid":"rs121908556","trait_name":"Normokalemic periodic paralysis, potassium-sensitive","url":"https://www.mygenelog.com/ko/variants/rs121908556"},{"risk_tier":"standard","rsid":"rs121908557","trait_name":"Normokalemic periodic paralysis, potassium-sensitive","url":"https://www.mygenelog.com/ko/variants/rs121908557"},{"risk_tier":"standard","rsid":"rs121908559","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs121908559"},{"risk_tier":"standard","rsid":"rs121908560","trait_name":"Paramyotonia congenita/hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs121908560"},{"risk_tier":"standard","rsid":"rs121908561","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs121908561"},{"risk_tier":"standard","rsid":"rs1224997537","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1224997537"},{"risk_tier":"standard","rsid":"rs1287863349","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs1287863349"},{"risk_tier":"standard","rsid":"rs1331907655","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1331907655"},{"risk_tier":"standard","rsid":"rs1358028812","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1358028812"},{"risk_tier":"standard","rsid":"rs1555600605","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1555600605"},{"risk_tier":"standard","rsid":"rs1555601448","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1555601448"},{"risk_tier":"standard","rsid":"rs1555603671","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1555603671"},{"risk_tier":"standard","rsid":"rs1567816461","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1567816461"},{"risk_tier":"standard","rsid":"rs1567816549","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1567816549"},{"risk_tier":"standard","rsid":"rs1567817380","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1567817380"},{"risk_tier":"standard","rsid":"rs1597978607","trait_name":"Arthrogryposis multiplex congenita","url":"https://www.mygenelog.com/ko/variants/rs1597978607"},{"risk_tier":"standard","rsid":"rs1597985462","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1597985462"},{"risk_tier":"standard","rsid":"rs1598405334","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1598405334"},{"risk_tier":"sensitive","rsid":"rs1598406692","trait_name":"Congenital myasthenic syndrome 16","url":"https://www.mygenelog.com/ko/variants/rs1598406692"},{"risk_tier":"standard","rsid":"rs1908593639","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1908593639"},{"risk_tier":"standard","rsid":"rs1908594231","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1908594231"},{"risk_tier":"sensitive","rsid":"rs1908668408","trait_name":"Congenital myasthenic syndrome 16","url":"https://www.mygenelog.com/ko/variants/rs1908668408"},{"risk_tier":"standard","rsid":"rs1908691206","trait_name":"SCN4A-related non-dystrophic myotonia","url":"https://www.mygenelog.com/ko/variants/rs1908691206"},{"risk_tier":"standard","rsid":"rs1909453191","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1909453191"},{"risk_tier":"standard","rsid":"rs1909519361","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs1909519361"},{"risk_tier":"standard","rsid":"rs2109079","trait_name":"Height (baseline)","url":"https://www.mygenelog.com/ko/variants/rs2109079"},{"risk_tier":"standard","rsid":"rs2144773878","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs2144773878"},{"risk_tier":"standard","rsid":"rs2144774834","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs2144774834"},{"risk_tier":"standard","rsid":"rs2144779553","trait_name":"SCN4A-related non-dystrophic myotonia","url":"https://www.mygenelog.com/ko/variants/rs2144779553"},{"risk_tier":"standard","rsid":"rs2144793242","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs2144793242"},{"risk_tier":"standard","rsid":"rs2144798676","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs2144798676"},{"risk_tier":"standard","rsid":"rs2144798704","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs2144798704"},{"risk_tier":"standard","rsid":"rs2509284285","trait_name":"Congenital myopathy 22B, severe fetal","url":"https://www.mygenelog.com/ko/variants/rs2509284285"},{"risk_tier":"standard","rsid":"rs2509285181","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs2509285181"},{"risk_tier":"standard","rsid":"rs2509285379","trait_name":"Congenital myopathy 22B, severe fetal","url":"https://www.mygenelog.com/ko/variants/rs2509285379"},{"risk_tier":"standard","rsid":"rs2509287979","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs2509287979"},{"risk_tier":"standard","rsid":"rs2509289236","trait_name":"Congenital myopathy 22B, severe fetal","url":"https://www.mygenelog.com/ko/variants/rs2509289236"},{"risk_tier":"standard","rsid":"rs2509290730","trait_name":"Congenital myopathy 22A, classic","url":"https://www.mygenelog.com/ko/variants/rs2509290730"},{"risk_tier":"standard","rsid":"rs2509291006","trait_name":"Potassium-aggravated myotonia","url":"https://www.mygenelog.com/ko/variants/rs2509291006"},{"risk_tier":"standard","rsid":"rs2509291040","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs2509291040"},{"risk_tier":"sensitive","rsid":"rs2509305424","trait_name":"SCN4A-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2509305424"},{"risk_tier":"standard","rsid":"rs2509308046","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs2509308046"},{"risk_tier":"standard","rsid":"rs2509313987","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs2509313987"},{"risk_tier":"standard","rsid":"rs2509315709","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs2509315709"},{"risk_tier":"standard","rsid":"rs2509317969","trait_name":"Congenital myopathy 22B, severe fetal","url":"https://www.mygenelog.com/ko/variants/rs2509317969"},{"risk_tier":"standard","rsid":"rs2509318035","trait_name":"Congenital myopathy 22A, classic","url":"https://www.mygenelog.com/ko/variants/rs2509318035"},{"risk_tier":"sensitive","rsid":"rs2509325722","trait_name":"SCN4A-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2509325722"},{"risk_tier":"standard","rsid":"rs2877372","trait_name":"Hip circumference adjusted for BMI","url":"https://www.mygenelog.com/ko/variants/rs2877372"},{"risk_tier":"standard","rsid":"rs4968680","trait_name":"Forced expiratory volume (baseline)","url":"https://www.mygenelog.com/ko/variants/rs4968680"},{"risk_tier":"standard","rsid":"rs527236148","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs527236148"},{"risk_tier":"standard","rsid":"rs527236150","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs527236150"},{"risk_tier":"standard","rsid":"rs557322255","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs557322255"},{"risk_tier":"standard","rsid":"rs749400108","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs749400108"},{"risk_tier":"standard","rsid":"rs75828444","trait_name":"Height (baseline)","url":"https://www.mygenelog.com/ko/variants/rs75828444"},{"risk_tier":"standard","rsid":"rs759347899","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs759347899"},{"risk_tier":"standard","rsid":"rs763893717","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs763893717"},{"risk_tier":"standard","rsid":"rs771340029","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs771340029"},{"risk_tier":"standard","rsid":"rs774453167","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs774453167"},{"risk_tier":"standard","rsid":"rs775244273","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs775244273"},{"risk_tier":"sensitive","rsid":"rs777998706","trait_name":"Congenital myasthenic syndrome 16","url":"https://www.mygenelog.com/ko/variants/rs777998706"},{"risk_tier":"standard","rsid":"rs780703403","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs780703403"},{"risk_tier":"standard","rsid":"rs80338784","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs80338784"},{"risk_tier":"standard","rsid":"rs80338785","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs80338785"},{"risk_tier":"standard","rsid":"rs80338788","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs80338788"},{"risk_tier":"standard","rsid":"rs80338789","trait_name":"Hypokalemic periodic paralysis, type 2","url":"https://www.mygenelog.com/ko/variants/rs80338789"},{"risk_tier":"standard","rsid":"rs80338792","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs80338792"},{"risk_tier":"standard","rsid":"rs80338955","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs80338955"},{"risk_tier":"standard","rsid":"rs80338956","trait_name":"Paramyotonia congenita of Von Eulenburg","url":"https://www.mygenelog.com/ko/variants/rs80338956"},{"risk_tier":"standard","rsid":"rs80338957","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs80338957"},{"risk_tier":"standard","rsid":"rs80338959","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs80338959"},{"risk_tier":"standard","rsid":"rs80338960","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs80338960"},{"risk_tier":"standard","rsid":"rs80338962","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs80338962"},{"risk_tier":"standard","rsid":"rs8074752","trait_name":"Aspartate aminotransferase levels","url":"https://www.mygenelog.com/ko/variants/rs8074752"},{"risk_tier":"standard","rsid":"rs864622785","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs864622785"},{"risk_tier":"standard","rsid":"rs865887222","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs865887222"},{"risk_tier":"sensitive","rsid":"rs867587467","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs867587467"},{"risk_tier":"sensitive","rsid":"rs879253789","trait_name":"Congenital myasthenic syndrome","url":"https://www.mygenelog.com/ko/variants/rs879253789"},{"risk_tier":"standard","rsid":"rs886041805","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs886041805"},{"risk_tier":"standard","rsid":"rs914586984","trait_name":"Potassium-aggravated myotonia","url":"https://www.mygenelog.com/ko/variants/rs914586984"},{"risk_tier":"standard","rsid":"rs943370469","trait_name":"Hyperkalemic periodic paralysis","url":"https://www.mygenelog.com/ko/variants/rs943370469"}]}
