{"most_severe_consequence":"intron_variant","evidence":["Multiple_observations"],"mappings":[{"ancestral_allele":null,"seq_region_name":"6","coord_system":"chromosome","start":39642997,"strand":1,"location":"6:39642997-39642997","allele_string":"A/G","end":39642997,"assembly_name":"GRCm39"}],"var_class":"SNP","name":"rs242617365","minor_allele":null,"MAF":null,"genotypes":[],"source":"Short variant data imported from EVA","synonyms":[],"ambiguity":"R"}