{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/NSD2","ko":"https://www.mygenelog.com/ko/api/v1/genes/NSD2"},"condition_count":1,"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":"NSD2","url":"https://www.mygenelog.com/genes/NSD2","variant_count":26,"variants":[{"risk_tier":"standard","rsid":"rs10006069","trait_name":"red cell diameter width (RDW, mean, inv-norm transformed)","url":"https://www.mygenelog.com/variants/rs10006069"},{"risk_tier":"standard","rsid":"rs10488835","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs10488835"},{"risk_tier":"standard","rsid":"rs114244559","trait_name":"Height (baseline)","url":"https://www.mygenelog.com/variants/rs114244559"},{"risk_tier":"standard","rsid":"rs114728242","trait_name":"red cell diameter width (RDW, minimum, inv-norm transformed)","url":"https://www.mygenelog.com/variants/rs114728242"},{"risk_tier":"standard","rsid":"rs142639234","trait_name":"Body shape phenotype PC2","url":"https://www.mygenelog.com/variants/rs142639234"},{"risk_tier":"sensitive","rsid":"rs1440755101","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs1440755101"},{"risk_tier":"sensitive","rsid":"rs1560602800","trait_name":"Wolf-Hirschhorn like syndrome","url":"https://www.mygenelog.com/variants/rs1560602800"},{"risk_tier":"sensitive","rsid":"rs1560635105","trait_name":"Wolf-Hirschhorn like syndrome","url":"https://www.mygenelog.com/variants/rs1560635105"},{"risk_tier":"sensitive","rsid":"rs1577434780","trait_name":"NSD2-related disorder","url":"https://www.mygenelog.com/variants/rs1577434780"},{"risk_tier":"sensitive","rsid":"rs1719469952","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1719469952"},{"risk_tier":"sensitive","rsid":"rs1726909627","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs1726909627"},{"risk_tier":"sensitive","rsid":"rs2108805626","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2108805626"},{"risk_tier":"sensitive","rsid":"rs2108950399","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2108950399"},{"risk_tier":"sensitive","rsid":"rs2108959336","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2108959336"},{"risk_tier":"sensitive","rsid":"rs2108971327","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2108971327"},{"risk_tier":"sensitive","rsid":"rs2108976771","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2108976771"},{"risk_tier":"sensitive","rsid":"rs2109020378","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2109020378"},{"risk_tier":"standard","rsid":"rs2187692","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs2187692"},{"risk_tier":"sensitive","rsid":"rs2474219766","trait_name":"NSD2-related disorder","url":"https://www.mygenelog.com/variants/rs2474219766"},{"risk_tier":"sensitive","rsid":"rs2474331632","trait_name":"4p partial monosomy syndrome","url":"https://www.mygenelog.com/variants/rs2474331632"},{"risk_tier":"sensitive","rsid":"rs2474621918","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2474621918"},{"risk_tier":"sensitive","rsid":"rs2474622067","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2474622067"},{"risk_tier":"sensitive","rsid":"rs2474633301","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2474633301"},{"risk_tier":"sensitive","rsid":"rs2474638543","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs2474638543"},{"risk_tier":"sensitive","rsid":"rs574794395","trait_name":"Rauch-Steindl syndrome","url":"https://www.mygenelog.com/variants/rs574794395"},{"risk_tier":"standard","rsid":"rs76475197","trait_name":"red cell diameter width (RDW, maximum, inv-norm transformed)","url":"https://www.mygenelog.com/variants/rs76475197"}]}