{"header":null,"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1439724792;vf=48291215\">rs1439724792</a>","entries":[{"key":"Class","value":"SNP"},{"key":"Source","value":"dbSNP"},{"value":"1:60297746","key":"Location"},{"value":"G/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=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1439724792;vf=48291215\">Explore this variant</a>"}],"highlight":""}]}