{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/COL27A1","ko":"https://www.mygenelog.com/ko/api/v1/genes/COL27A1"},"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":"COL27A1","url":"https://www.mygenelog.com/ko/genes/COL27A1","variant_count":32,"variants":[{"risk_tier":"standard","rsid":"rs10982102","trait_name":"Standing height (UKB data field 50)","url":"https://www.mygenelog.com/ko/variants/rs10982102"},{"risk_tier":"standard","rsid":"rs112446757","trait_name":"ORM1 protein levels","url":"https://www.mygenelog.com/ko/variants/rs112446757"},{"risk_tier":"sensitive","rsid":"rs1220881640","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1220881640"},{"risk_tier":"standard","rsid":"rs1249741","trait_name":"Appendicular lean mass","url":"https://www.mygenelog.com/ko/variants/rs1249741"},{"risk_tier":"sensitive","rsid":"rs1289391715","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1289391715"},{"risk_tier":"sensitive","rsid":"rs1328051341","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1328051341"},{"risk_tier":"sensitive","rsid":"rs1401322428","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1401322428"},{"risk_tier":"sensitive","rsid":"rs140950220","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs140950220"},{"risk_tier":"sensitive","rsid":"rs1465820080","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1465820080"},{"risk_tier":"sensitive","rsid":"rs1554816354","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1554816354"},{"risk_tier":"sensitive","rsid":"rs1554821679","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1554821679"},{"risk_tier":"sensitive","rsid":"rs1554829390","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1554829390"},{"risk_tier":"sensitive","rsid":"rs1830319943","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1830319943"},{"risk_tier":"sensitive","rsid":"rs1830954329","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1830954329"},{"risk_tier":"sensitive","rsid":"rs1848097390","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1848097390"},{"risk_tier":"sensitive","rsid":"rs1849088219","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs1849088219"},{"risk_tier":"standard","rsid":"rs2014134","trait_name":"ORM1 protein levels","url":"https://www.mygenelog.com/ko/variants/rs2014134"},{"risk_tier":"sensitive","rsid":"rs2135594366","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs2135594366"},{"risk_tier":"sensitive","rsid":"rs2490550913","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs2490550913"},{"risk_tier":"standard","rsid":"rs2567707","trait_name":"Pulse pressure","url":"https://www.mygenelog.com/ko/variants/rs2567707"},{"risk_tier":"standard","rsid":"rs34986757","trait_name":"Alanine aminotransferase levels","url":"https://www.mygenelog.com/ko/variants/rs34986757"},{"risk_tier":"standard","rsid":"rs4143245","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs4143245"},{"risk_tier":"standard","rsid":"rs4978569","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs4978569"},{"risk_tier":"standard","rsid":"rs4979352","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs4979352"},{"risk_tier":"standard","rsid":"rs528148931","trait_name":"Glycosphingolipids (d42:2) levels","url":"https://www.mygenelog.com/ko/variants/rs528148931"},{"risk_tier":"standard","rsid":"rs7019849","trait_name":"Physical function (baseline)","url":"https://www.mygenelog.com/ko/variants/rs7019849"},{"risk_tier":"sensitive","rsid":"rs737142","trait_name":"Osteoarthritis of the hip or knee (with total joint replacement)","url":"https://www.mygenelog.com/ko/variants/rs737142"},{"risk_tier":"standard","rsid":"rs747771422","trait_name":"Spinal cord injury without evidence of spinal bone injury (PheCode 952)","url":"https://www.mygenelog.com/ko/variants/rs747771422"},{"risk_tier":"sensitive","rsid":"rs753461513","trait_name":"Steel syndrome","url":"https://www.mygenelog.com/ko/variants/rs753461513"},{"risk_tier":"sensitive","rsid":"rs760476125","trait_name":"Familial cancer of breast","url":"https://www.mygenelog.com/ko/variants/rs760476125"},{"risk_tier":"sensitive","rsid":"rs7868992","trait_name":"Tourette syndrome","url":"https://www.mygenelog.com/ko/variants/rs7868992"},{"risk_tier":"standard","rsid":"rs956743578","trait_name":"Glycosphingolipids (d42:2) levels","url":"https://www.mygenelog.com/ko/variants/rs956743578"}]}