{"mappings":[{"strand":1,"end":230710048,"coord_system":"chromosome","seq_region_name":"1","allele_string":"A/G","ancestral_allele":"G","location":"1:230710048-230710048","assembly_name":"GRCh38","start":230710048}],"var_class":"SNP","synonyms":["106150.0001","PA166153539","VAR_007096","rs3182295","rs4714","rs17856353","rs61617185","rs386606420","RCV000019693","VCV000018068","RCV000405686","RCV000019691","RCV000242838","RCV002259306","RCV000835695","RCV000019692","NM_001382817.1:c.803T>C","NM_001384479.1:c.776T>C","NM_000029.4:c.803T>C","NP_001371408.1:p.Met259Thr","NP_001369746.2:p.Met259Thr","NM_000029.3:c.803T>C","NM_001382817.2:c.776T>C","NM_001382817.3:c.776T>C"],"genotyping_chips":["Illumina_HumanHap550","Illumina_HumanHap650Y","Illumina_ImmunoChip","HumanCoreExome-12","Illumina_HumanOmni2.5","Illumina_ExomeChip","Illumina_HumanOmni1-Quad","Illumina_1M-duo","Illumina_Human660W-quad","Illumina_Human610_Quad","HumanOmniExpress"],"ambiguity":"R","minor_allele":null,"most_severe_consequence":"missense_variant","name":"rs699","clinical_significance":["benign"],"MAF":null,"source":"Variants (including SNPs and indels) imported from dbSNP","evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"]}