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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":"MYO6","url":"https://www.mygenelog.com/ko/genes/MYO6","variant_count":36,"variants":[{"risk_tier":"standard","rsid":"rs1057523846","trait_name":"Autosomal recessive nonsyndromic hearing loss 37","url":"https://www.mygenelog.com/ko/variants/rs1057523846"},{"risk_tier":"standard","rsid":"rs1060499799","trait_name":"Autosomal dominant nonsyndromic hearing loss 22","url":"https://www.mygenelog.com/ko/variants/rs1060499799"},{"risk_tier":"standard","rsid":"rs10943287","trait_name":"Height (baseline)","url":"https://www.mygenelog.com/ko/variants/rs10943287"},{"risk_tier":"standard","rsid":"rs121912557","trait_name":"Autosomal dominant nonsyndromic hearing loss 22","url":"https://www.mygenelog.com/ko/variants/rs121912557"},{"risk_tier":"standard","rsid":"rs121912558","trait_name":"Autosomal recessive 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