{"database":"EVA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Vcf":["ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB51904/SNP_BHMTBHMT2.vcf.gz.tbi","ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB51904/SNP_BHMTBHMT2.vcf.gz.csi","ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB51904/SNP_BHMTBHMT2.vcf.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":0,"searchCount":0},"additional":{"dataset_type":["Genotyping By Array"],"omics_type":["Genomics"],"submitter":["Xiangya School of Public Health, Department of Epidemiology and Health Statistics"],"instrument_platform":["Illumina MiniSeq"],"species":["Homo Sapiens"],"full_dataset_link":["https://www.ebi.ac.uk/eva/?eva-study=PRJEB51904"],"repository":["EVA"],"name_synonyms":["Heart, Congenital Heart Defect, Congenital Heart Diseases, Disease, Malformation Of Hearts, Malformation Of, HEL-S-61p, congenital heart, heart-congenital defect, heart abnormalities, Abnormality, Congenital Heart, Defects, defect, congenital., Defect, Heart Abnormalities, Heart Abnormality, Heart Defect, Congenital Heart Disease, Congenital, heart abnormality, abnormalities, Malformation Of Heart, BHMT1, Associations, heart defect, heart, Heart Disease, Congenital Heart Defects, defects, malformation Of"],"description_synonyms":["Heart, Congenital Heart Defect, Dmel_CG6393, DmelCG42257, cg11478, Congenital Heart Diseases, Disease, coronary arteriosclerosis, Malformation Of Hearts, Malformation Of, CDH, HEL-S-61p, congenital heart, heart-congenital defect, heart abnormalities, Defects, Congenital Heart, Abnormality, CHD., defect, CG30327, Heart Abnormalities, Defect, Heart Abnormality, Heart Defect, chd, X-chordin, CG11478, Congenital Heart Disease, Congenital, heart abnormality, 1.1.99.1, abnormalities, Malformation Of Heart, BHMT1, congenital, 65K, CG6393, heart defect, heart, Heart Disease, CG42257, Dmel_CG30327, snp, Congenital Heart Defects, defects, malformation Of, Chd"],"citation_count":["0"],"additional_accession":[]},"is_claimable":false,"name":"Association of maternal BHMT and BHMT2 gene polymorphism and congenital heart disease in offspring","description":"A project aimed to explore significant SNP of maternal BHMT and BHMT2 gene related to CHD","dates":{"publication":"2022-03-27"},"accession":"PRJEB51904","cross_references":{"TAXONOMY":["9606"]}}