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