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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":"NR2E3","url":"https://www.mygenelog.com/ko/genes/NR2E3","variant_count":33,"variants":[{"risk_tier":"sensitive","rsid":"rs104894492","trait_name":"Enhanced S-cone syndrome","url":"https://www.mygenelog.com/ko/variants/rs104894492"},{"risk_tier":"sensitive","rsid":"rs104894493","trait_name":"Enhanced S-cone syndrome","url":"https://www.mygenelog.com/ko/variants/rs104894493"},{"risk_tier":"standard","rsid":"rs121912631","trait_name":"Retinitis pigmentosa 37","url":"https://www.mygenelog.com/ko/variants/rs121912631"},{"risk_tier":"standard","rsid":"rs1257334132","trait_name":"Retinitis pigmentosa","url":"https://www.mygenelog.com/ko/variants/rs1257334132"},{"risk_tier":"sensitive","rsid":"rs1269569810","trait_name":"NR2E3-related 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