{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/DYNC1H1","ko":"https://www.mygenelog.com/ko/api/v1/genes/DYNC1H1"},"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":"DYNC1H1","url":"https://www.mygenelog.com/ko/genes/DYNC1H1","variant_count":88,"variants":[{"risk_tier":"standard","rsid":"rs1057518083","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures","url":"https://www.mygenelog.com/ko/variants/rs1057518083"},{"risk_tier":"sensitive","rsid":"rs1057518287","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs1057518287"},{"risk_tier":"standard","rsid":"rs1057518961","trait_name":"Global developmental delay","url":"https://www.mygenelog.com/ko/variants/rs1057518961"},{"risk_tier":"standard","rsid":"rs1064796765","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs1064796765"},{"risk_tier":"standard","rsid":"rs1236304133","trait_name":"Intellectual disability","url":"https://www.mygenelog.com/ko/variants/rs1236304133"},{"risk_tier":"sensitive","rsid":"rs1327664377","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs1327664377"},{"risk_tier":"sensitive","rsid":"rs1351401023","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs1351401023"},{"risk_tier":"sensitive","rsid":"rs1370693832","trait_name":"DYNC1H1-related disorder","url":"https://www.mygenelog.com/ko/variants/rs1370693832"},{"risk_tier":"standard","rsid":"rs13749","trait_name":"Platelet count (UKB data field 30080)","url":"https://www.mygenelog.com/ko/variants/rs13749"},{"risk_tier":"sensitive","rsid":"rs1421708361","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs1421708361"},{"risk_tier":"sensitive","rsid":"rs1429535306","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs1429535306"},{"risk_tier":"standard","rsid":"rs143265607","trait_name":"Serum levels of protein C6orf226","url":"https://www.mygenelog.com/ko/variants/rs143265607"},{"risk_tier":"standard","rsid":"rs1555408333","trait_name":"Neuronopathy, distal hereditary motor, autosomal dominant","url":"https://www.mygenelog.com/ko/variants/rs1555408333"},{"risk_tier":"sensitive","rsid":"rs1555408819","trait_name":"Hereditary motor neuron disease","url":"https://www.mygenelog.com/ko/variants/rs1555408819"},{"risk_tier":"sensitive","rsid":"rs1555408829","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1555408829"},{"risk_tier":"standard","rsid":"rs1555409836","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs1555409836"},{"risk_tier":"sensitive","rsid":"rs1555410010","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1555410010"},{"risk_tier":"standard","rsid":"rs1555411305","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs1555411305"},{"risk_tier":"standard","rsid":"rs1555411378","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs1555411378"},{"risk_tier":"standard","rsid":"rs1555411394","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs1555411394"},{"risk_tier":"sensitive","rsid":"rs1567018763","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1567018763"},{"risk_tier":"sensitive","rsid":"rs1567019064","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs1567019064"},{"risk_tier":"sensitive","rsid":"rs1595597572","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs1595597572"},{"risk_tier":"standard","rsid":"rs1595599240","trait_name":"Neuronopathy, distal hereditary motor, autosomal dominant","url":"https://www.mygenelog.com/ko/variants/rs1595599240"},{"risk_tier":"standard","rsid":"rs1595600898","trait_name":"Neuronopathy, distal hereditary motor, autosomal dominant","url":"https://www.mygenelog.com/ko/variants/rs1595600898"},{"risk_tier":"standard","rsid":"rs1595605449","trait_name":"Lower limb muscle weakness","url":"https://www.mygenelog.com/ko/variants/rs1595605449"},{"risk_tier":"standard","rsid":"rs1595609005","trait_name":"Intellectual disability","url":"https://www.mygenelog.com/ko/variants/rs1595609005"},{"risk_tier":"standard","rsid":"rs1595629181","trait_name":"Intellectual disability","url":"https://www.mygenelog.com/ko/variants/rs1595629181"},{"risk_tier":"standard","rsid":"rs2047850664","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2047850664"},{"risk_tier":"sensitive","rsid":"rs2047931446","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2047931446"},{"risk_tier":"sensitive","rsid":"rs2047932647","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2047932647"},{"risk_tier":"standard","rsid":"rs2047935205","trait_name":"Lissencephaly","url":"https://www.mygenelog.com/ko/variants/rs2047935205"},{"risk_tier":"standard","rsid":"rs2047938879","trait_name":"Lissencephaly","url":"https://www.mygenelog.com/ko/variants/rs2047938879"},{"risk_tier":"standard","rsid":"rs2047950288","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2047950288"},{"risk_tier":"standard","rsid":"rs2047998539","trait_name":"Intellectual disability","url":"https://www.mygenelog.com/ko/variants/rs2047998539"},{"risk_tier":"standard","rsid":"rs2048322542","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2048322542"},{"risk_tier":"standard","rsid":"rs2048519381","trait_name":"Lissencephaly","url":"https://www.mygenelog.com/ko/variants/rs2048519381"},{"risk_tier":"standard","rsid":"rs2048611744","trait_name":"Lissencephaly","url":"https://www.mygenelog.com/ko/variants/rs2048611744"},{"risk_tier":"sensitive","rsid":"rs2141272574","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2141272574"},{"risk_tier":"sensitive","rsid":"rs2141274671","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2141274671"},{"risk_tier":"standard","rsid":"rs2141274749","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures","url":"https://www.mygenelog.com/ko/variants/rs2141274749"},{"risk_tier":"standard","rsid":"rs2141280750","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures","url":"https://www.mygenelog.com/ko/variants/rs2141280750"},{"risk_tier":"standard","rsid":"rs2141280974","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures","url":"https://www.mygenelog.com/ko/variants/rs2141280974"},{"risk_tier":"standard","rsid":"rs2152577516","trait_name":"Abnormal cerebral morphology","url":"https://www.mygenelog.com/ko/variants/rs2152577516"},{"risk_tier":"standard","rsid":"rs2152579365","trait_name":"Intellectual disability","url":"https://www.mygenelog.com/ko/variants/rs2152579365"},{"risk_tier":"standard","rsid":"rs2152589131","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2152589131"},{"risk_tier":"standard","rsid":"rs2152590264","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2152590264"},{"risk_tier":"standard","rsid":"rs2152592151","trait_name":"Neurodevelopmental delay","url":"https://www.mygenelog.com/ko/variants/rs2152592151"},{"risk_tier":"sensitive","rsid":"rs2152592202","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2152592202"},{"risk_tier":"sensitive","rsid":"rs2152594747","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2152594747"},{"risk_tier":"standard","rsid":"rs2152596521","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2152596521"},{"risk_tier":"sensitive","rsid":"rs2503693934","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2503693934"},{"risk_tier":"sensitive","rsid":"rs2503714640","trait_name":"DYNC1H1-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2503714640"},{"risk_tier":"sensitive","rsid":"rs2503714817","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2503714817"},{"risk_tier":"sensitive","rsid":"rs2503715379","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2503715379"},{"risk_tier":"sensitive","rsid":"rs2503715383","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2503715383"},{"risk_tier":"sensitive","rsid":"rs2503726588","trait_name":"DYNC1H1-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2503726588"},{"risk_tier":"standard","rsid":"rs2503727339","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2503727339"},{"risk_tier":"standard","rsid":"rs2503727356","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2503727356"},{"risk_tier":"sensitive","rsid":"rs2503730449","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs2503730449"},{"risk_tier":"sensitive","rsid":"rs2503731165","trait_name":"Autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs2503731165"},{"risk_tier":"standard","rsid":"rs2503734461","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2503734461"},{"risk_tier":"sensitive","rsid":"rs2503742080","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs2503742080"},{"risk_tier":"sensitive","rsid":"rs2503751910","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs2503751910"},{"risk_tier":"standard","rsid":"rs2503757710","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2503757710"},{"risk_tier":"standard","rsid":"rs2503757868","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2503757868"},{"risk_tier":"standard","rsid":"rs2503773145","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs2503773145"},{"risk_tier":"sensitive","rsid":"rs2503806504","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2503806504"},{"risk_tier":"sensitive","rsid":"rs2503812014","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs2503812014"},{"risk_tier":"sensitive","rsid":"rs387906738","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs387906738"},{"risk_tier":"standard","rsid":"rs387906743","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures","url":"https://www.mygenelog.com/ko/variants/rs387906743"},{"risk_tier":"standard","rsid":"rs397509411","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs397509411"},{"risk_tier":"standard","rsid":"rs397509412","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs397509412"},{"risk_tier":"standard","rsid":"rs587780564","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures","url":"https://www.mygenelog.com/ko/variants/rs587780564"},{"risk_tier":"sensitive","rsid":"rs713993043","trait_name":"Charcot-Marie-Tooth disease axonal type 2O","url":"https://www.mygenelog.com/ko/variants/rs713993043"},{"risk_tier":"standard","rsid":"rs727505393","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures","url":"https://www.mygenelog.com/ko/variants/rs727505393"},{"risk_tier":"standard","rsid":"rs757725348","trait_name":"Lissencephaly","url":"https://www.mygenelog.com/ko/variants/rs757725348"},{"risk_tier":"sensitive","rsid":"rs797044901","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs797044901"},{"risk_tier":"sensitive","rsid":"rs797044928","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs797044928"},{"risk_tier":"standard","rsid":"rs797045177","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs797045177"},{"risk_tier":"standard","rsid":"rs797045178","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs797045178"},{"risk_tier":"standard","rsid":"rs797045529","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs797045529"},{"risk_tier":"standard","rsid":"rs863223361","trait_name":"Abnormality of neuronal migration","url":"https://www.mygenelog.com/ko/variants/rs863223361"},{"risk_tier":"standard","rsid":"rs869312693","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs869312693"},{"risk_tier":"sensitive","rsid":"rs879253881","trait_name":"DYNC1H1-related neurodevelopmental disorders","url":"https://www.mygenelog.com/ko/variants/rs879253881"},{"risk_tier":"standard","rsid":"rs879253971","trait_name":"Cortical dysplasia, complex, with other brain malformations 13","url":"https://www.mygenelog.com/ko/variants/rs879253971"},{"risk_tier":"standard","rsid":"rs879254085","trait_name":"Neuronopathy, distal hereditary motor, autosomal dominant","url":"https://www.mygenelog.com/ko/variants/rs879254085"},{"risk_tier":"sensitive","rsid":"rs879254267","trait_name":"DYNC1H1-related disorder","url":"https://www.mygenelog.com/ko/variants/rs879254267"}]}
