[{"end":68699593,"id":"rs1228327172","strand":1,"start":68699593,"feature_type":"variation","assembly_name":"GRCh37","source":"dbSNP","alleles":["T","C"],"seq_region_name":"14","consequence_type":"intron_variant","clinical_significance":[]},{"start":68699594,"feature_type":"variation","strand":1,"end":68699594,"id":"CR129920","consequence_type":"intron_variant","clinical_significance":[],"seq_region_name":"14","alleles":["HGMD_MUTATION"],"assembly_name":"GRCh37","source":"HGMD-PUBLIC"},{"source":"dbSNP","assembly_name":"GRCh37","alleles":["C","T"],"seq_region_name":"14","clinical_significance":[],"consequence_type":"intron_variant","id":"rs1314913","end":68699594,"strand":1,"feature_type":"variation","start":68699594},{"strand":1,"feature_type":"variation","start":68699596,"end":68699596,"id":"rs2080175389","seq_region_name":"14","clinical_significance":[],"consequence_type":"intron_variant","source":"dbSNP","assembly_name":"GRCh37","alleles":["T","C"]}]