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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":"MITF","url":"https://www.mygenelog.com/ko/genes/MITF","variant_count":82,"variants":[{"risk_tier":"sensitive","rsid":"rs104893744","trait_name":"Waardenburg syndrome type 2A","url":"https://www.mygenelog.com/ko/variants/rs104893744"},{"risk_tier":"sensitive","rsid":"rs104893745","trait_name":"Tietz syndrome","url":"https://www.mygenelog.com/ko/variants/rs104893745"},{"risk_tier":"sensitive","rsid":"rs104893746","trait_name":"Waardenburg syndrome type 2A","url":"https://www.mygenelog.com/ko/variants/rs104893746"},{"risk_tier":"sensitive","rsid":"rs1057517966","trait_name":"Waardenburg syndrome type 2A","url":"https://www.mygenelog.com/ko/variants/rs1057517966"},{"risk_tier":"standard","rsid":"rs1057519325","trait_name":"Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and 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