GWAS summary data tables

Fadista J et al. Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis. Human Molecular Genetics 2019; 28(2): 332-340

We are releasing the summary statistics from our genome-wide meta-analysis of Infantile Hypertrophic Pyloric Stenosis (IHPS) disease. The meta-analysis includes a total of 1395 cases and 4438 controls of Danish ancestry (from two cohorts). The file includes 6,576,307 autosomal SNPs (MAF>1%) directly genotyped or imputed to the Haplotype Reference Consortium (imputation info score ≥ 0.8).

The file contains:

  • CHR – chromosome of the genetic variant (hg19 assembly)
  • SNP - dbSNP v146 variant ID
  • BP – base-pair position of the genetic variant (hg19 assembly)
  • A1 – effect allele
  • A2 – other allele
  • OR – odds-ratio for the effect allele
  • SE – standard error
  • P – fixed-effects meta-analysis p-value
  • Q - p-value for Cochrane's Q statistic (measure of heterogeneity between the two cohorts)

Acknowledging the data

When using data from the downloadable GWAS summary results please acknowledge the source of the data as follows:

Data on IHPS disease GWAS have been contributed by Statens Serum Institut investigators and have been downloaded from https://www.danishnationalbiobank.com/GWAS.

In addition to the above acknowledgement, please cite the paper:

Fadista J et al. Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis. Human Molecular Genetics 2019; 28(2): 332-340.

Downloading the data

biobanks.dk/GWAS/MEGA_CIDR_IHPS_summaryStats.txt.gz

Disclaimer

These data are provided "as is" and without warranty, for scientific and educational use only. The authors assume no responsibility for errors or omissions. If you download these data, you acknowledge that these data will be used only for non-commercial research purposes; that the investigator is in compliance with all laws or regulations and institutional policies regarding human subjects and genetics research; and that secondary distribution of the data is prohibited. The authors shall not be held liable for any use or misuse of the data.