{"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs2089666022;vdb=variation;vf=178999799\">rs2089666022</a>","highlight":"","entries":[{"value":"SNP","key":"Class"},{"key":"Source","value":"dbSNP"},{"value":"2:207615901","key":"Location"},{"key":"Alleles","value":"C/T (Forward strand)"},{"value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#02599c\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant occurring within an intron\">intron variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#32cd32\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant of a non coding RNA gene\">non coding transcript variant</span></nobr><li></ul>","key":"Consequences"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs2089666022;vdb=variation;vf=178999799\">Explore this variant</a>","key":null},{"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs2089666022;vdb=variation;vf=178999799\">Gene/Transcript Locations</a>","key":null}]}],"header":null}