{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/GREB1L","ko":"https://www.mygenelog.com/ko/api/v1/genes/GREB1L"},"condition_count":1,"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":"GREB1L","url":"https://www.mygenelog.com/ko/genes/GREB1L","variant_count":29,"variants":[{"risk_tier":"standard","rsid":"rs111293916","trait_name":"Estimated glomerular filtration rate (creatinine)","url":"https://www.mygenelog.com/ko/variants/rs111293916"},{"risk_tier":"standard","rsid":"rs1208372191","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs1208372191"},{"risk_tier":"standard","rsid":"rs1212136611","trait_name":"Male infertility with azoospermia or oligozoospermia due to single gene mutation","url":"https://www.mygenelog.com/ko/variants/rs1212136611"},{"risk_tier":"standard","rsid":"rs1254264958","trait_name":"Male infertility with azoospermia or oligozoospermia due to single gene mutation","url":"https://www.mygenelog.com/ko/variants/rs1254264958"},{"risk_tier":"standard","rsid":"rs1268367147","trait_name":"1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) levels","url":"https://www.mygenelog.com/ko/variants/rs1268367147"},{"risk_tier":"sensitive","rsid":"rs1377926237","trait_name":"Mayer-Rokitansky-K\u00fcster-Hauser syndrome type 2","url":"https://www.mygenelog.com/ko/variants/rs1377926237"},{"risk_tier":"standard","rsid":"rs1555648043","trait_name":"Inner ear malformation","url":"https://www.mygenelog.com/ko/variants/rs1555648043"},{"risk_tier":"standard","rsid":"rs1555650110","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs1555650110"},{"risk_tier":"standard","rsid":"rs1555659101","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs1555659101"},{"risk_tier":"standard","rsid":"rs1555661490","trait_name":"Inner ear malformation","url":"https://www.mygenelog.com/ko/variants/rs1555661490"},{"risk_tier":"standard","rsid":"rs1555661907","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs1555661907"},{"risk_tier":"standard","rsid":"rs1555662027","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs1555662027"},{"risk_tier":"standard","rsid":"rs1555662052","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs1555662052"},{"risk_tier":"standard","rsid":"rs1555662061","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs1555662061"},{"risk_tier":"standard","rsid":"rs1555664772","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs1555664772"},{"risk_tier":"standard","rsid":"rs2033773650","trait_name":"Profound hearing impairment","url":"https://www.mygenelog.com/ko/variants/rs2033773650"},{"risk_tier":"standard","rsid":"rs2036715609","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs2036715609"},{"risk_tier":"standard","rsid":"rs2036991057","trait_name":"Congenital anomaly of kidney and urinary tract","url":"https://www.mygenelog.com/ko/variants/rs2036991057"},{"risk_tier":"standard","rsid":"rs2037388926","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs2037388926"},{"risk_tier":"standard","rsid":"rs2037623971","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs2037623971"},{"risk_tier":"standard","rsid":"rs2144522176","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs2144522176"},{"risk_tier":"standard","rsid":"rs2145813286","trait_name":"Hearing loss, autosomal dominant 80","url":"https://www.mygenelog.com/ko/variants/rs2145813286"},{"risk_tier":"standard","rsid":"rs2146025908","trait_name":"Hearing loss, autosomal dominant 80","url":"https://www.mygenelog.com/ko/variants/rs2146025908"},{"risk_tier":"standard","rsid":"rs2511868849","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs2511868849"},{"risk_tier":"sensitive","rsid":"rs2511993759","trait_name":"GREB1L-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2511993759"},{"risk_tier":"standard","rsid":"rs4377239","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs4377239"},{"risk_tier":"standard","rsid":"rs561529182","trait_name":"Renal hypodysplasia/aplasia 3","url":"https://www.mygenelog.com/ko/variants/rs561529182"},{"risk_tier":"standard","rsid":"rs72882867","trait_name":"Appendicular lean mass","url":"https://www.mygenelog.com/ko/variants/rs72882867"},{"risk_tier":"standard","rsid":"rs8098861","trait_name":"Non-albumin protein levels","url":"https://www.mygenelog.com/ko/variants/rs8098861"}]}