{"ambiguity":"R","source":"Variants (including SNPs and indels) imported from dbSNP","phenotypes":[{"variants":null,"genes":"AGT","source":"ClinVar","trait":"ClinVar: phenotype not specified","risk_allele":"G"},{"ontology_accessions":["EFO:0000378","EFO:0001645","HP:0001677"],"source":"NHGRI-EBI GWAS catalog","genes":"AGT","beta_coefficient":"0.036 unit decrease","study":"PMID:29212778","pvalue":"2.00e-8","risk_allele":"A","trait":"Coronary Artery Disease","variants":"rs699"},{"source":"NHGRI-EBI GWAS catalog","genes":null,"ontology_accessions":["EFO:0006336","EFO:0006945"],"risk_allele":"G","pvalue":"7.00e-46","study":"PMID:38689001","beta_coefficient":"0.2164 unit increase","variants":"rs699","trait":"Diastolic blood pressure"},{"ontology_accessions":["EFO:0006336","EFO:0006945"],"genes":null,"source":"NHGRI-EBI GWAS catalog","trait":"Diastolic blood pressure","variants":"rs699","pvalue":"7.00e-25","beta_coefficient":"0.2195 unit decrease","study":"PMID:35762941","risk_allele":"A"},{"pvalue":"7.00e-38","study":"PMID:39537608","beta_coefficient":"0.022419937 unit increase","risk_allele":"G","trait":"Diastolic blood pressure MTAG","variants":"rs699","ontology_accessions":["EFO:0006336"],"genes":null,"source":"NHGRI-EBI GWAS catalog"},{"risk_allele":"G","ontology_accessions":["MONDO:0007781"],"trait":"Hypertension, essential, susceptibility to","genes":"AGT","source":"ClinVar","variants":null},{"trait":"Hypertensive disorder","ontology_accessions":["EFO:0000537","MONDO:0005044"],"variants":null,"source":"ClinVar","genes":"AGT","risk_allele":"G"},{"beta_coefficient":"0.32885453 unit decrease","study":"PMID:27618448","pvalue":"4.00e-12","risk_allele":"A","trait":"Mean arterial pressure","variants":"rs699","ontology_accessions":["EFO:0006340"],"genes":"AGT","source":"NHGRI-EBI GWAS catalog"},{"variants":"rs699","trait":"Pulse pressure","risk_allele":"G","beta_coefficient":"0.1186 unit increase","study":"PMID:38689001","pvalue":"1.00e-11","genes":null,"source":"NHGRI-EBI GWAS catalog","ontology_accessions":["EFO:0005763"]},{"variants":null,"genes":"AGT","source":"ClinVar","ontology_accessions":["HP:0008660","MONDO:0017609","Orphanet:3033"],"trait":"RENAL TUBULAR DYSGENESIS","risk_allele":"G"},{"trait":"Systolic blood pressure","variants":"rs699","pvalue":"3.00e-19","beta_coefficient":"0.3311 unit decrease","study":"PMID:35762941","risk_allele":"A","ontology_accessions":["EFO:0006335","EFO:0006944"],"source":"NHGRI-EBI GWAS catalog","genes":null},{"trait":"Systolic blood pressure","variants":"rs699","pvalue":"8.00e-41","study":"PMID:38689001","beta_coefficient":"0.327 unit increase","risk_allele":"G","ontology_accessions":["EFO:0006335","EFO:0006944"],"source":"NHGRI-EBI GWAS catalog","genes":null},{"ontology_accessions":["EFO:0006335","EFO:0006944"],"genes":"AGT","source":"NHGRI-EBI GWAS catalog","trait":"Systolic blood pressure","variants":"rs699","pvalue":"6.00e-26","beta_coefficient":"0.2918 mmHg decrease","study":"PMID:30578418","risk_allele":"A"},{"genes":null,"source":"NHGRI-EBI GWAS catalog","ontology_accessions":["EFO:0006335"],"risk_allele":"G","study":"PMID:39537608","beta_coefficient":"0.020998787 unit increase","pvalue":"5.00e-33","variants":"rs699","trait":"Systolic blood pressure MTAG"}],"most_severe_consequence":"missense_variant","minor_allele":null,"synonyms":["rs4714","rs61617185","rs17856353","rs3182295","rs386606420","RCV002259306","RCV000405686","RCV000835695","RCV000019691","VCV000018068","RCV000019692","RCV000019693","RCV000242838","NM_001382817.1:c.803T>C","NM_001384479.1:c.776T>C","NP_001369746.2:p.Met259Thr","NM_001382817.2:c.776T>C","NM_001382817.3:c.776T>C","NM_000029.4:c.803T>C","NM_000029.3:c.803T>C","NP_001371408.1:p.Met259Thr","106150.0001","VAR_007096","PA166153539"],"name":"rs699","clinical_significance":["benign"],"mappings":[{"coord_system":"chromosome","strand":1,"assembly_name":"GRCh38","start":230710048,"location":"1:230710048-230710048","allele_string":"A/G","seq_region_name":"1","ancestral_allele":"G","end":230710048}],"MAF":null,"var_class":"SNP","evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"]}