{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/CDH2","ko":"https://www.mygenelog.com/ko/api/v1/genes/CDH2"},"condition_count":6,"drug_count":0,"lang":"en","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":"CDH2","url":"https://www.mygenelog.com/genes/CDH2","variant_count":27,"variants":[{"risk_tier":"standard","rsid":"rs11083244","trait_name":"Spherical equivalent","url":"https://www.mygenelog.com/variants/rs11083244"},{"risk_tier":"standard","rsid":"rs11083300","trait_name":"PR interval","url":"https://www.mygenelog.com/variants/rs11083300"},{"risk_tier":"standard","rsid":"rs111852224","trait_name":"Educational attainment (MTAG)","url":"https://www.mygenelog.com/variants/rs111852224"},{"risk_tier":"standard","rsid":"rs11564336","trait_name":"Aortic stenosis","url":"https://www.mygenelog.com/variants/rs11564336"},{"risk_tier":"standard","rsid":"rs11665344","trait_name":"Electrocardiogram morphology (amplitude at temporal datapoints)","url":"https://www.mygenelog.com/variants/rs11665344"},{"risk_tier":"standard","rsid":"rs117905482","trait_name":"CDH2 protein levels","url":"https://www.mygenelog.com/variants/rs117905482"},{"risk_tier":"standard","rsid":"rs1220027","trait_name":"Educational attainment (years of education)","url":"https://www.mygenelog.com/variants/rs1220027"},{"risk_tier":"standard","rsid":"rs12458840","trait_name":"Aortic stenosis","url":"https://www.mygenelog.com/variants/rs12458840"},{"risk_tier":"standard","rsid":"rs1555630396","trait_name":"Cerebral arteriovenous malformation","url":"https://www.mygenelog.com/variants/rs1555630396"},{"risk_tier":"standard","rsid":"rs1599010918","trait_name":"Axon pathfinding, cardiac, ocular and genital defects","url":"https://www.mygenelog.com/variants/rs1599010918"},{"risk_tier":"standard","rsid":"rs1599011050","trait_name":"Axon pathfinding, cardiac, ocular and genital defects","url":"https://www.mygenelog.com/variants/rs1599011050"},{"risk_tier":"standard","rsid":"rs1599017933","trait_name":"Axon pathfinding, cardiac, ocular and genital defects","url":"https://www.mygenelog.com/variants/rs1599017933"},{"risk_tier":"standard","rsid":"rs17446505","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs17446505"},{"risk_tier":"standard","rsid":"rs17446692","trait_name":"Highest math class taken","url":"https://www.mygenelog.com/variants/rs17446692"},{"risk_tier":"standard","rsid":"rs17468213","trait_name":"Refractive error","url":"https://www.mygenelog.com/variants/rs17468213"},{"risk_tier":"standard","rsid":"rs17468924","trait_name":"CDH2 protein levels","url":"https://www.mygenelog.com/variants/rs17468924"},{"risk_tier":"sensitive","rsid":"rs199984052","trait_name":"CDH2-related disorder","url":"https://www.mygenelog.com/variants/rs199984052"},{"risk_tier":"sensitive","rsid":"rs2013040501","trait_name":"Agenesis of corpus callosum, cardiac, ocular, and genital syndrome","url":"https://www.mygenelog.com/variants/rs2013040501"},{"risk_tier":"sensitive","rsid":"rs2013111940","trait_name":"Agenesis of corpus callosum, cardiac, ocular, and genital syndrome","url":"https://www.mygenelog.com/variants/rs2013111940"},{"risk_tier":"standard","rsid":"rs201775968","trait_name":"Axon pathfinding, cardiac, ocular and genital defects","url":"https://www.mygenelog.com/variants/rs201775968"},{"risk_tier":"standard","rsid":"rs2143975765","trait_name":"Arrhythmogenic right ventricular dysplasia, familial, 14","url":"https://www.mygenelog.com/variants/rs2143975765"},{"risk_tier":"standard","rsid":"rs2510799501","trait_name":"Arrhythmogenic right ventricular dysplasia, familial, 14","url":"https://www.mygenelog.com/variants/rs2510799501"},{"risk_tier":"sensitive","rsid":"rs2510816952","trait_name":"Attention deficit-hyperactivity disorder 8","url":"https://www.mygenelog.com/variants/rs2510816952"},{"risk_tier":"standard","rsid":"rs7243759","trait_name":"Educational attainment","url":"https://www.mygenelog.com/variants/rs7243759"},{"risk_tier":"standard","rsid":"rs754880999","trait_name":"Corpus callosum, agenesis of","url":"https://www.mygenelog.com/variants/rs754880999"},{"risk_tier":"standard","rsid":"rs777374626","trait_name":"Auditory neuropathy","url":"https://www.mygenelog.com/variants/rs777374626"},{"risk_tier":"standard","rsid":"rs965753331","trait_name":"Arrhythmogenic right ventricular dysplasia, familial, 14","url":"https://www.mygenelog.com/variants/rs965753331"}]}