[{"allele_string":"C/A/T","colocated_variants":[{"start":5976110,"seq_region_name":"12","end":5976110,"strand":1,"id":"CS066320","phenotype_or_disease":1,"allele_string":"HGMD_MUTATION"},{"strand":1,"clin_sig_allele":"T:not_provided","start":5976110,"end":5976110,"seq_region_name":"12","clin_sig":["not_provided"],"allele_string":"C/A/T","clin_sig_ref_allele":"C","var_synonyms":{"ClinVar":["RCV000086885","VCV000100472"]},"id":"rs61751290","phenotype_or_disease":1}],"end":5976110,"id":"rs61751290","seq_region_name":"12","strand":1,"transcript_consequences":[{"impact":"HIGH","variant_allele":"A","gene_id":"ENSG00000110799","gene_symbol_source":"HGNC","gene_symbol":"VWF","transcript_id":"ENST00000261405","hgnc_id":"HGNC:12726","biotype":"protein_coding","strand":-1,"consequence_terms":["splice_donor_variant"]},{"variant_allele":"T","impact":"HIGH","transcript_id":"ENST00000261405","gene_symbol":"VWF","gene_symbol_source":"HGNC","gene_id":"ENSG00000110799","strand":-1,"biotype":"protein_coding","hgnc_id":"HGNC:12726","consequence_terms":["splice_donor_variant"]},{"strand":-1,"hgnc_id":"HGNC:12726","biotype":"protein_coding","consequence_terms":["splice_donor_variant"],"variant_allele":"A","impact":"HIGH","gene_symbol_source":"HGNC","gene_symbol":"VWF","transcript_id":"ENST00000895679","gene_id":"ENSG00000110799"},{"impact":"HIGH","variant_allele":"T","gene_id":"ENSG00000110799","transcript_id":"ENST00000895679","gene_symbol":"VWF","gene_symbol_source":"HGNC","hgnc_id":"HGNC:12726","biotype":"protein_coding","strand":-1,"consequence_terms":["splice_donor_variant"]},{"consequence_terms":["intron_variant"],"strand":-1,"hgnc_id":"HGNC:12726","biotype":"protein_coding","gene_symbol":"VWF","transcript_id":"ENST00000895680","gene_symbol_source":"HGNC","gene_id":"ENSG00000110799","variant_allele":"A","impact":"MODIFIER"},{"variant_allele":"T","impact":"MODIFIER","gene_symbol":"VWF","transcript_id":"ENST00000895680","gene_symbol_source":"HGNC","gene_id":"ENSG00000110799","strand":-1,"hgnc_id":"HGNC:12726","biotype":"protein_coding","consequence_terms":["intron_variant"]},{"strand":-1,"hgnc_id":"HGNC:12726","biotype":"protein_coding","consequence_terms":["splice_donor_variant"],"variant_allele":"A","impact":"HIGH","gene_symbol":"VWF","transcript_id":"ENST00001139594","gene_symbol_source":"HGNC","gene_id":"ENSG00000110799"},{"impact":"HIGH","variant_allele":"T","gene_id":"ENSG00000110799","transcript_id":"ENST00001139594","gene_symbol":"VWF","gene_symbol_source":"HGNC","biotype":"protein_coding","hgnc_id":"HGNC:12726","strand":-1,"consequence_terms":["splice_donor_variant"]}],"most_severe_consequence":"splice_donor_variant","start":5976110,"input":"rs61751290","assembly_name":"GRCh38"}]