{"features":[{"entries":[{"key":"Class","value":"SNP"},{"key":"Source","value":"dbSNP"},{"value":"2:192108177","key":"Location"},{"value":"A/G (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"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs984568939;vf=110812162\">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=rs984568939;vf=110812162\">Gene/Transcript Locations</a>","key":null}],"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs984568939;vf=110812162\">rs984568939</a>"},{"entries":[{"value":"SNP","key":"Class"},{"value":"dbSNP","key":"Source"},{"key":"Location","value":"2:51028318"},{"key":"Alleles","value":"T/G (Forward strand)"},{"key":"Consequences","value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#7ac5cd\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A UTR variant of the 5' UTR\">5 prime UTR variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#a52a2a\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant located within a regulatory region\">regulatory region variant</span></nobr><li></ul>"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs984568959;vf=110812164\">Explore this variant</a>","key":null}],"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs984568959;vf=110812164\">rs984568959</a>"},{"entries":[{"key":"Class","value":"SNP"},{"key":"Source","value":"dbSNP"},{"key":"Location","value":"2:81352649"},{"value":"A/G (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=rs1672816985;vf=155590199\">Explore this variant</a>"}],"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1672816985;vf=155590199\">rs1672816985</a>"}],"header":null}