{"features":[{"highlight":"","entries":[{"key":"Class","value":"SNP"},{"value":"dbSNP","key":"Source"},{"key":"Location","value":"2:137525110"},{"value":"T/C (Forward strand)","key":"Alleles"},{"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></ul>","key":"Consequences"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs987771032;vf=111089999\">Explore this variant</a>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs987771032;vf=111089999\">Gene/Transcript Locations</a>"}],"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs987771032;vf=111089999\">rs987771032</a>"}],"header":null}