{"minor_allele":null,"MAF":null,"clinical_significance":["association"],"evidence":["Frequency","1000Genomes","Cited","Phenotype_or_Disease","TOPMed","gnomAD"],"synonyms":["601806.0001","VCV000007685","RCV000008124"],"most_severe_consequence":"intron_variant","mappings":[{"ancestral_allele":"G","strand":1,"location":"2:135851076-135851076","allele_string":"G/A/C/T","start":135851076,"end":135851076,"assembly_name":"GRCh38","coord_system":"chromosome","seq_region_name":"2"}],"ambiguity":"N","name":"rs4988235","var_class":"SNP","source":"Variants (including SNPs and indels) imported from dbSNP"}