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