Genomics

Dataset Information

0

Association of maternal BHMT and BHMT2 gene polymorphism and congenital heart disease in offspring

ABSTRACT: A project aimed to explore significant SNP of maternal BHMT and BHMT2 gene related to CHD

INSTRUMENT(S): Illumina MiniSeq

ORGANISM(S): Homo Sapiens

SUBMITTER: Xiangya School of Public Health, Department of Epidemiology and Health Statistics 

PROVIDER: PRJEB51904 | EVA | 2022-03-27

REPOSITORIES: EVA

Json Xml

Dataset's files

Source:
Action DRS
SNP_BHMTBHMT2.vcf.gz Vcf
SNP_BHMTBHMT2.vcf.gz.csi Vcf
SNP_BHMTBHMT2.vcf.gz.tbi Vcf
Items per page:
1 - 3 of 3

Similar Datasets

Genomics Association of MTR gene polymorphisms and congenital heart disease
2022-07-25 | PRJEB54935 | EVA
Unknown Correlation between GATA4 gene polymorphism and congenital heart disease.
| S-EPMC4659101 | biostudies-literature
Unknown Association of MTHFD1 G1958A (rs2236225) gene polymorphism with the risk of congenital heart disease: a systematic review and meta-analysis.
| S-EPMC11771109 | biostudies-literature
Unknown Association between MTR A2756G polymorphism and susceptibility to congenital heart disease: A meta-analysis.
| S-EPMC9269412 | biostudies-literature
Genomics Gene sequences of significant human-skin related bacterial isolates
| PRJEB85951 | ENA
Unknown Association study of polymorphism in Thrombomodulin gene [rs1042579] with cardiovascular disease.
| S-EPMC8823559 | biostudies-literature
Unknown Association of maternal folic acid supplementation and offspring MTRR gene polymorphism with congenital heart disease: a hospital-based case-control study in Han population.
| S-EPMC11660932 | biostudies-literature
Unknown Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.
| S-EPMC4713608 | biostudies-literature
Unknown The MALAT1 gene polymorphism and its relationship with the onset of congenital heart disease in Chinese.
| S-EPMC6048208 | biostudies-literature
Transcriptomics Inflammatory gene expression profiling in peripheral blood from patients with Alzheimer’s disease reveals key pathways and hub genes with potential diagnostic utility
2021-03-13 | GSE168813 | GEO