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