{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/ADNP","ko":"https://www.mygenelog.com/ko/api/v1/genes/ADNP"},"condition_count":2,"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":"ADNP","url":"https://www.mygenelog.com/ko/genes/ADNP","variant_count":23,"variants":[{"risk_tier":"standard","rsid":"rs1057518991","trait_name":"Autism, severe","url":"https://www.mygenelog.com/ko/variants/rs1057518991"},{"risk_tier":"sensitive","rsid":"rs1135401791","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs1135401791"},{"risk_tier":"sensitive","rsid":"rs1221864735","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs1221864735"},{"risk_tier":"standard","rsid":"rs12479470","trait_name":"Age at menopause","url":"https://www.mygenelog.com/ko/variants/rs12479470"},{"risk_tier":"standard","rsid":"rs150215935","trait_name":"Smoking initiation","url":"https://www.mygenelog.com/ko/variants/rs150215935"},{"risk_tier":"sensitive","rsid":"rs1555810308","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1555810308"},{"risk_tier":"sensitive","rsid":"rs1555812161","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1555812161"},{"risk_tier":"sensitive","rsid":"rs1568710501","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs1568710501"},{"risk_tier":"sensitive","rsid":"rs1600934347","trait_name":"ADNP-related disorder","url":"https://www.mygenelog.com/ko/variants/rs1600934347"},{"risk_tier":"sensitive","rsid":"rs1981068436","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs1981068436"},{"risk_tier":"sensitive","rsid":"rs1981147033","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs1981147033"},{"risk_tier":"sensitive","rsid":"rs2122743080","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs2122743080"},{"risk_tier":"sensitive","rsid":"rs2122743549","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs2122743549"},{"risk_tier":"sensitive","rsid":"rs2515578225","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs2515578225"},{"risk_tier":"sensitive","rsid":"rs2515579204","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs2515579204"},{"risk_tier":"sensitive","rsid":"rs2515581500","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs2515581500"},{"risk_tier":"sensitive","rsid":"rs2515592600","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs2515592600"},{"risk_tier":"sensitive","rsid":"rs587777524","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs587777524"},{"risk_tier":"sensitive","rsid":"rs587777526","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs587777526"},{"risk_tier":"standard","rsid":"rs6096186","trait_name":"CES3 protein levels","url":"https://www.mygenelog.com/ko/variants/rs6096186"},{"risk_tier":"sensitive","rsid":"rs779340209","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs779340209"},{"risk_tier":"sensitive","rsid":"rs886041116","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs886041116"},{"risk_tier":"sensitive","rsid":"rs886056775","trait_name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs886056775"}]}