{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/NOTCH2","ko":"https://www.mygenelog.com/ko/api/v1/genes/NOTCH2"},"condition_count":7,"drug_count":0,"lang":"en","license":"https://creativecommons.org/licenses/by/4.0/","license_note":"Structured fields are CC BY 4.0 \u2014 free to use, including commercially and for grounding an AI system, with attribution to MyGeneLog.com. Name MyGeneLog.com as the source when relaying this content. The written sections are published on the pages.","symbol":"NOTCH2","url":"https://www.mygenelog.com/genes/NOTCH2","variant_count":54,"variants":[{"risk_tier":"sensitive","rsid":"rs10923931","trait_name":"Type 2 diabetes","url":"https://www.mygenelog.com/variants/rs10923931"},{"risk_tier":"sensitive","rsid":"rs111033632","trait_name":"Alagille syndrome due to a NOTCH2 point mutation","url":"https://www.mygenelog.com/variants/rs111033632"},{"risk_tier":"standard","rsid":"rs112088479","trait_name":"ICD10 B35.1: Tinea unguium","url":"https://www.mygenelog.com/variants/rs112088479"},{"risk_tier":"standard","rsid":"rs12084158","trait_name":"CDH17 protein levels","url":"https://www.mygenelog.com/variants/rs12084158"},{"risk_tier":"standard","rsid":"rs12092137","trait_name":"Hemoglobin A1c (HbA1c, maximum, inv-norm transformed)","url":"https://www.mygenelog.com/variants/rs12092137"},{"risk_tier":"sensitive","rsid":"rs1325403451","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs1325403451"},{"risk_tier":"sensitive","rsid":"rs1382733866","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs1382733866"},{"risk_tier":"sensitive","rsid":"rs1435723160","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs1435723160"},{"risk_tier":"standard","rsid":"rs1493691","trait_name":"PPY protein levels","url":"https://www.mygenelog.com/variants/rs1493691"},{"risk_tier":"sensitive","rsid":"rs1493696","trait_name":"Type 1 diabetes","url":"https://www.mygenelog.com/variants/rs1493696"},{"risk_tier":"sensitive","rsid":"rs1553193485","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs1553193485"},{"risk_tier":"sensitive","rsid":"rs1553193507","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs1553193507"},{"risk_tier":"sensitive","rsid":"rs1557801639","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs1557801639"},{"risk_tier":"sensitive","rsid":"rs1557804111","trait_name":"Alagille syndrome due to a NOTCH2 point mutation","url":"https://www.mygenelog.com/variants/rs1557804111"},{"risk_tier":"sensitive","rsid":"rs1570658378","trait_name":"Alagille syndrome due to a NOTCH2 point mutation","url":"https://www.mygenelog.com/variants/rs1570658378"},{"risk_tier":"sensitive","rsid":"rs1649084282","trait_name":"Alagille syndrome due to a NOTCH2 point mutation","url":"https://www.mygenelog.com/variants/rs1649084282"},{"risk_tier":"sensitive","rsid":"rs1649088431","trait_name":"Alagille syndrome due to a NOTCH2 point mutation","url":"https://www.mygenelog.com/variants/rs1649088431"},{"risk_tier":"sensitive","rsid":"rs1649449471","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs1649449471"},{"risk_tier":"sensitive","rsid":"rs1650362306","trait_name":"Alagille syndrome due to a NOTCH2 point mutation","url":"https://www.mygenelog.com/variants/rs1650362306"},{"risk_tier":"sensitive","rsid":"rs2101098803","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs2101098803"},{"risk_tier":"sensitive","rsid":"rs2101139955","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs2101139955"},{"risk_tier":"sensitive","rsid":"rs2101141863","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs2101141863"},{"risk_tier":"sensitive","rsid":"rs2101142159","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs2101142159"},{"risk_tier":"standard","rsid":"rs2453042","trait_name":"Nevus count or cutaneous melanoma","url":"https://www.mygenelog.com/variants/rs2453042"},{"risk_tier":"sensitive","rsid":"rs2453044","trait_name":"Systemic lupus erythematosus (MTAG)","url":"https://www.mygenelog.com/variants/rs2453044"},{"risk_tier":"sensitive","rsid":"rs2453051","trait_name":"Type 2 diabetes","url":"https://www.mygenelog.com/variants/rs2453051"},{"risk_tier":"sensitive","rsid":"rs2493394","trait_name":"Type 2 diabetes","url":"https://www.mygenelog.com/variants/rs2493394"},{"risk_tier":"standard","rsid":"rs2493413","trait_name":"PNLIPRP1 protein levels","url":"https://www.mygenelog.com/variants/rs2493413"},{"risk_tier":"sensitive","rsid":"rs2526103665","trait_name":"NOTCH2-related disorder","url":"https://www.mygenelog.com/variants/rs2526103665"},{"risk_tier":"sensitive","rsid":"rs2526105966","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs2526105966"},{"risk_tier":"sensitive","rsid":"rs2526112692","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs2526112692"},{"risk_tier":"sensitive","rsid":"rs2526112913","trait_name":"Alagille syndrome due to a NOTCH2 point mutation","url":"https://www.mygenelog.com/variants/rs2526112913"},{"risk_tier":"sensitive","rsid":"rs2526313922","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs2526313922"},{"risk_tier":"standard","rsid":"rs2603961","trait_name":"White blood cell count","url":"https://www.mygenelog.com/variants/rs2603961"},{"risk_tier":"sensitive","rsid":"rs28516010","trait_name":"Type 2 diabetes","url":"https://www.mygenelog.com/variants/rs28516010"},{"risk_tier":"sensitive","rsid":"rs312262798","trait_name":"Alagille syndrome due to a NOTCH2 point mutation","url":"https://www.mygenelog.com/variants/rs312262798"},{"risk_tier":"sensitive","rsid":"rs312262801","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs312262801"},{"risk_tier":"standard","rsid":"rs327189","trait_name":"CRYBB2 protein levels","url":"https://www.mygenelog.com/variants/rs327189"},{"risk_tier":"standard","rsid":"rs327200","trait_name":"Lymphocyte count","url":"https://www.mygenelog.com/variants/rs327200"},{"risk_tier":"standard","rsid":"rs375724393","trait_name":"Free Cholesterol to Cholesteryl Esters in Small HDL ratio","url":"https://www.mygenelog.com/variants/rs375724393"},{"risk_tier":"sensitive","rsid":"rs387906746","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs387906746"},{"risk_tier":"sensitive","rsid":"rs387906747","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs387906747"},{"risk_tier":"sensitive","rsid":"rs387906748","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs387906748"},{"risk_tier":"sensitive","rsid":"rs387906749","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs387906749"},{"risk_tier":"standard","rsid":"rs41302079","trait_name":"QRS duration","url":"https://www.mygenelog.com/variants/rs41302079"},{"risk_tier":"standard","rsid":"rs699779","trait_name":"Glucose (fasting status unknown, mean, inv-norm transformed)","url":"https://www.mygenelog.com/variants/rs699779"},{"risk_tier":"sensitive","rsid":"rs72697237","trait_name":"Type 2 diabetes with neurological manifestations (PheCode 250.24)","url":"https://www.mygenelog.com/variants/rs72697237"},{"risk_tier":"standard","rsid":"rs72697266","trait_name":"Glycated hemoglobin levels","url":"https://www.mygenelog.com/variants/rs72697266"},{"risk_tier":"standard","rsid":"rs77542178","trait_name":"ACP6 protein levels","url":"https://www.mygenelog.com/variants/rs77542178"},{"risk_tier":"sensitive","rsid":"rs782059779","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs782059779"},{"risk_tier":"standard","rsid":"rs782423173","trait_name":"NOTCH2 protein levels","url":"https://www.mygenelog.com/variants/rs782423173"},{"risk_tier":"standard","rsid":"rs835574","trait_name":"White blood cell count","url":"https://www.mygenelog.com/variants/rs835574"},{"risk_tier":"sensitive","rsid":"rs835576","trait_name":"Type 2 diabetes","url":"https://www.mygenelog.com/variants/rs835576"},{"risk_tier":"sensitive","rsid":"rs886041862","trait_name":"Hajdu-Cheney syndrome","url":"https://www.mygenelog.com/variants/rs886041862"}]}
