[{"allele_string":"G/C","transcript_consequences":[{"biotype":"protein_coding","impact":"MODIFIER","transcript_id":"ENST00000379370","gene_symbol":"AGRN","strand":1,"distance":226,"gene_id":"ENSG00000188157","gene_symbol_source":"HGNC","hgnc_id":329,"variant_allele":"C","consequence_terms":["upstream_gene_variant"]}],"strand":1,"most_severe_consequence":"upstream_gene_variant","id":"rs901011140","input":"rs901011140","colocated_variants":[{"frequencies":{"C":{"gnomadg_remaining":0.0004826,"gnomadg_sas":0,"gnomadg_ami":0,"gnomadg_mid":0,"gnomadg_asj":0,"gnomadg_afr":0.0002677,"gnomadg_amr":6.626e-05,"gnomadg":8.696e-05,"gnomadg_fin":0,"gnomadg_eas":0,"gnomadg_nfe":0}},"start":955277,"seq_region_name":"1","end":955277,"allele_string":"G/C","id":"rs901011140","strand":1}],"regulatory_feature_consequences":[{"regulatory_feature_id":"ENSR1_9DX4","biotype":"promoter","impact":"MODIFIER","variant_allele":"C","consequence_terms":["regulatory_region_variant"]}],"assembly_name":"GRCh37","start":955277,"end":955277,"seq_region_name":"1"}]