[{"assembly_name":"GRCh37","end":22125503,"strand":1,"start":22125503,"seq_region_name":"9","allele_string":"G/C","colocated_variants":[{"allele_string":"G/C","id":"rs1333049","pubmed":[27386823,26950853,26958643,28209224,19501493,22042884,21860704,21149552,20159871,19474294,21894447,21971053,21804106,20502693,22199011,18224312,22400124,18533027,27424552,18852197,21297524,28813480,22403240,22856518,26677855,27015805,23963167,19343170,20386740,21400687,24728607,20017983,24573017,24607648,28979897,20549515,22144573,22623978,22029572,27892471,18362232,19173706,19214202,26252781,20435227,26999117,21606135,19924713,19955471,19956433,25717410,27153677,24098343,18780302,18675980,19475673,20231156,20858905,21152093,21698238,24906238,28400043,17634449,18979498,19164808,19207022,19750184,20098575,20981302,21242481,21369780,22295058,22848412,25617895,23729007,18469204,20605023,21372283,26729200,27249003,22429504,26483964,18704761,23870195,23587283,24926413,27736948,19463184,24676469,26789557,28138111,27096864,27507036,27004807,21424681,20175863,22505696,19559344,19578366,23142796,19171343,24246088,18987759,19819472,19926059,21375403,21385355,21705410,24777168,25105296,27317124,27721851,26982883,1988832],"frequencies":{"C":{"sas":0.4908,"eas":0.5367,"afr":0.2133,"eur":0.4722,"amr":0.4553}},"strand":1,"start":22125503,"seq_region_name":"9","phenotype_or_disease":1,"minor_allele_freq":0.4181,"minor_allele":"C","end":22125503}],"id":"9:g.22125503G>C","most_severe_consequence":"downstream_gene_variant","transcript_consequences":[{"biotype":"antisense","gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","variant_allele":"C","impact":"MODIFIER","gene_symbol":"CDKN2B-AS1","consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000422420","hgnc_id":34341,"strand":1,"distance":4407},{"gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","biotype":"antisense","impact":"MODIFIER","gene_symbol":"CDKN2B-AS1","variant_allele":"C","consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000428597","strand":1,"distance":4409,"hgnc_id":34341},{"distance":4932,"strand":1,"hgnc_id":34341,"transcript_id":"ENST00000577551","consequence_terms":["downstream_gene_variant"],"gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","variant_allele":"C","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","biotype":"antisense"},{"impact":"MODIFIER","gene_symbol":"CDKN2B-AS1","variant_allele":"C","gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","biotype":"antisense","strand":1,"distance":4858,"hgnc_id":34341,"consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000580576"},{"consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000581051","hgnc_id":34341,"strand":1,"distance":4932,"biotype":"antisense","gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","variant_allele":"C","impact":"MODIFIER","gene_symbol":"CDKN2B-AS1"},{"consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000582072","strand":1,"distance":4932,"hgnc_id":34341,"gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","biotype":"antisense","impact":"MODIFIER","gene_symbol":"CDKN2B-AS1","variant_allele":"C"},{"distance":4932,"strand":1,"hgnc_id":34341,"transcript_id":"ENST00000584020","consequence_terms":["downstream_gene_variant"],"gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","variant_allele":"C","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","biotype":"antisense"},{"variant_allele":"C","gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","biotype":"antisense","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","hgnc_id":34341,"distance":4932,"strand":1,"transcript_id":"ENST00000584637","consequence_terms":["downstream_gene_variant"]},{"distance":4932,"strand":1,"hgnc_id":34341,"transcript_id":"ENST00000584816","consequence_terms":["downstream_gene_variant"],"gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","variant_allele":"C","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","biotype":"antisense"},{"biotype":"antisense","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","variant_allele":"C","gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","transcript_id":"ENST00000585267","consequence_terms":["downstream_gene_variant"],"hgnc_id":34341,"distance":4960,"strand":1}],"input":"9:g.22125503G>C"}]