{"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs1349680932;vdb=variation;vf=133185509\">rs1349680932</a>","highlight":"","entries":[{"value":"SNP","key":"Class"},{"key":"Source","value":"dbSNP"},{"value":"2:23714637","key":"Location"},{"value":"T/C (Forward strand)","key":"Alleles"},{"key":"Consequences","value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#636363\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant located in the intergenic region, between genes\">intergenic variant</span></nobr><li></ul>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs1349680932;vdb=variation;vf=133185509\">Explore this variant</a>"}]}],"header":null}