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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":"MED12","url":"https://www.mygenelog.com/ko/genes/MED12","variant_count":45,"variants":[{"risk_tier":"sensitive","rsid":"rs1057519381","trait_name":"FG syndrome 1","url":"https://www.mygenelog.com/ko/variants/rs1057519381"},{"risk_tier":"sensitive","rsid":"rs1085307941","trait_name":"Blepharophimosis - intellectual disability syndrome, MKB type","url":"https://www.mygenelog.com/ko/variants/rs1085307941"},{"risk_tier":"sensitive","rsid":"rs1556334519","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1556334519"},{"risk_tier":"sensitive","rsid":"rs1556334969","trait_name":"FG syndrome 1","url":"https://www.mygenelog.com/ko/variants/rs1556334969"},{"risk_tier":"sensitive","rsid":"rs1556337063","trait_name":"FG syndrome 1","url":"https://www.mygenelog.com/ko/variants/rs1556337063"},{"risk_tier":"sensitive","rsid":"rs1556340124","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1556340124"},{"risk_tier":"sensitive","rsid":"rs1569481124","trait_name":"FG syndrome 1","url":"https://www.mygenelog.com/ko/variants/rs1569481124"},{"risk_tier":"standard","rsid":"rs1569482431","trait_name":"Familial thoracic aortic aneurysm and aortic dissection","url":"https://www.mygenelog.com/ko/variants/rs1569482431"},{"risk_tier":"sensitive","rsid":"rs1602299778","trait_name":"FG syndrome 1","url":"https://www.mygenelog.com/ko/variants/rs1602299778"},{"risk_tier":"standard","rsid":"rs2092303356","trait_name":"X-linked intellectual disability with marfanoid habitus","url":"https://www.mygenelog.com/ko/variants/rs2092303356"},{"risk_tier":"standard","rsid":"rs2092313037","trait_name":"Familial thoracic aortic aneurysm and aortic dissection","url":"https://www.mygenelog.com/ko/variants/rs2092313037"},{"risk_tier":"sensitive","rsid":"rs2092317530","trait_name":"FG syndrome","url":"https://www.mygenelog.com/ko/variants/rs2092317530"},{"risk_tier":"standard","rsid":"rs2092347488","trait_name":"X-linked intellectual disability with marfanoid habitus","url":"https://www.mygenelog.com/ko/variants/rs2092347488"},{"risk_tier":"sensitive","rsid":"rs2147769775","trait_name":"FG syndrome","url":"https://www.mygenelog.com/ko/variants/rs2147769775"},{"risk_tier":"sensitive","rsid":"rs2147774632","trait_name":"FG syndrome 1","url":"https://www.mygenelog.com/ko/variants/rs2147774632"},{"risk_tier":"sensitive","rsid":"rs2147782173","trait_name":"Blepharophimosis - 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