{"features":[{"highlight":"","entries":[{"value":"SNP","key":"Class"},{"value":"dbSNP","key":"Source"},{"key":"Location","value":"2:26970673"},{"value":"C/T (Forward strand)","key":"Alleles"},{"key":"Consequences","value":"- 5 prime UTR variant
- non coding transcript exon variant
- intron variant
- non coding transcript variant
- regulatory region variant
"},{"value":"Explore this variant","key":null},{"key":null,"value":"Gene/Transcript Locations"}],"caption":"Variation: rs984568954"},{"highlight":"","caption":"Variation: rs1574652970","entries":[{"key":"Class","value":"SNP"},{"value":"dbSNP","key":"Source"},{"value":"2:230996455","key":"Location"},{"value":"A/C (Forward strand)","key":"Alleles"},{"value":"- synonymous variant
- intron variant
- NMD transcript variant
- regulatory region variant
","key":"Consequences"},{"value":"Explore this variant","key":null}]},{"highlight":"","caption":"Variation: rs1571546121","entries":[{"key":"Class","value":"SNP"},{"key":"Source","value":"dbSNP"},{"key":"Location","value":"1:201853026"},{"key":"Alleles","value":"A/C (Forward strand)"},{"key":"Consequences","value":"- missense variant
- non coding transcript exon variant
"},{"key":null,"value":"Explore this variant"}]}],"header":null}