{"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs1399672598;vdb=variation;vf=223138856\">rs1399672598</a>","highlight":"","entries":[{"value":"SNP","key":"Class"},{"key":"Source","value":"dbSNP"},{"key":"Location","value":"3:180676155"},{"key":"Alleles","value":"A/T (Forward strand)"},{"key":"Consequences","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>"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs1399672598;vdb=variation;vf=223138856\">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=rs1399672598;vdb=variation;vf=223138856\">Gene/Transcript Locations</a>","key":null}]}],"header":null}