{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/TCTN1","ko":"https://www.mygenelog.com/ko/api/v1/genes/TCTN1"},"condition_count":4,"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":"TCTN1","url":"https://www.mygenelog.com/ko/genes/TCTN1","variant_count":25,"variants":[{"risk_tier":"sensitive","rsid":"rs1165243207","trait_name":"Joubert syndrome 13","url":"https://www.mygenelog.com/ko/variants/rs1165243207"},{"risk_tier":"sensitive","rsid":"rs1303964272","trait_name":"Joubert syndrome","url":"https://www.mygenelog.com/ko/variants/rs1303964272"},{"risk_tier":"sensitive","rsid":"rs1307879089","trait_name":"TCTN1-related disorder","url":"https://www.mygenelog.com/ko/variants/rs1307879089"},{"risk_tier":"sensitive","rsid":"rs1475200635","trait_name":"Meckel-Gruber syndrome","url":"https://www.mygenelog.com/ko/variants/rs1475200635"},{"risk_tier":"standard","rsid":"rs1502337","trait_name":"Aortic stenosis","url":"https://www.mygenelog.com/ko/variants/rs1502337"},{"risk_tier":"sensitive","rsid":"rs1593376626","trait_name":"Joubert syndrome 13","url":"https://www.mygenelog.com/ko/variants/rs1593376626"},{"risk_tier":"sensitive","rsid":"rs200241085","trait_name":"Joubert syndrome 13","url":"https://www.mygenelog.com/ko/variants/rs200241085"},{"risk_tier":"sensitive","rsid":"rs200863258","trait_name":"Joubert syndrome and related disorders","url":"https://www.mygenelog.com/ko/variants/rs200863258"},{"risk_tier":"sensitive","rsid":"rs2066300090","trait_name":"Meckel-Gruber syndrome","url":"https://www.mygenelog.com/ko/variants/rs2066300090"},{"risk_tier":"sensitive","rsid":"rs2066444872","trait_name":"Joubert syndrome","url":"https://www.mygenelog.com/ko/variants/rs2066444872"},{"risk_tier":"sensitive","rsid":"rs2066579666","trait_name":"Meckel-Gruber syndrome","url":"https://www.mygenelog.com/ko/variants/rs2066579666"},{"risk_tier":"sensitive","rsid":"rs2067211703","trait_name":"Joubert syndrome and related disorders","url":"https://www.mygenelog.com/ko/variants/rs2067211703"},{"risk_tier":"sensitive","rsid":"rs2136045792","trait_name":"TCTN1-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2136045792"},{"risk_tier":"sensitive","rsid":"rs2548884767","trait_name":"TCTN1-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2548884767"},{"risk_tier":"sensitive","rsid":"rs2548929536","trait_name":"Joubert syndrome","url":"https://www.mygenelog.com/ko/variants/rs2548929536"},{"risk_tier":"sensitive","rsid":"rs367543065","trait_name":"Joubert syndrome 13","url":"https://www.mygenelog.com/ko/variants/rs367543065"},{"risk_tier":"sensitive","rsid":"rs374065616","trait_name":"Joubert syndrome","url":"https://www.mygenelog.com/ko/variants/rs374065616"},{"risk_tier":"standard","rsid":"rs61942627","trait_name":"Systolic blood pressure (MTAG)","url":"https://www.mygenelog.com/ko/variants/rs61942627"},{"risk_tier":"standard","rsid":"rs730882221","trait_name":"Global developmental delay","url":"https://www.mygenelog.com/ko/variants/rs730882221"},{"risk_tier":"sensitive","rsid":"rs748215804","trait_name":"Joubert syndrome","url":"https://www.mygenelog.com/ko/variants/rs748215804"},{"risk_tier":"sensitive","rsid":"rs751962801","trait_name":"Joubert syndrome 13","url":"https://www.mygenelog.com/ko/variants/rs751962801"},{"risk_tier":"sensitive","rsid":"rs756402483","trait_name":"Meckel-Gruber syndrome","url":"https://www.mygenelog.com/ko/variants/rs756402483"},{"risk_tier":"sensitive","rsid":"rs760922371","trait_name":"Joubert syndrome 13","url":"https://www.mygenelog.com/ko/variants/rs760922371"},{"risk_tier":"sensitive","rsid":"rs769457761","trait_name":"Joubert syndrome","url":"https://www.mygenelog.com/ko/variants/rs769457761"},{"risk_tier":"sensitive","rsid":"rs886039436","trait_name":"Joubert syndrome 13","url":"https://www.mygenelog.com/ko/variants/rs886039436"}]}
