{"genotyping_chips":["HumanCoreExome-12","Illumina_HumanOmni2.5","Illumina_ImmunoChip","Illumina_HumanHap650Y","Illumina_Human610_Quad","Illumina_1M-duo","Illumina_ExomeChip","Illumina_Human660W-quad","Illumina_HumanOmni1-Quad","Illumina_HumanHap550","HumanOmniExpress"],"source":"Variants (including SNPs and indels) imported from dbSNP","minor_allele":"A","evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"var_class":"SNP","ambiguity":"R","clinical_significance":["benign","risk factor"],"most_severe_consequence":"missense_variant","MAF":0.2949,"mappings":[{"allele_string":"A/G","coord_system":"chromosome","start":230710048,"location":"1:230710048-230710048","strand":1,"ancestral_allele":"G","seq_region_name":"1","end":230710048,"assembly_name":"GRCh38"}],"name":"rs699","synonyms":["VAR_007096","106150.0001","rs17856353","rs386606420","rs3182295","rs61617185","rs4714","RCV000405686","VCV000018068","RCV000835695","RCV000242838","RCV000019691","RCV000019692","RCV000019693","NP_000020.1:p.Met268Thr","NM_000029.3:c.803T>C","NM_000029.4:c.803T>C","PA166153539"]}