ID
45449
Beskrivning
Principal Investigator: David A. Schwartz, MD, University of Colorado, Denver - Aurora, CO, USA MeSH: Lung Diseases, Interstitial,Idiopathic Interstitial Pneumonias,Idiopathic Pulmonary Fibrosis,Familial Idiopathic Pulmonary Fibrosis https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000751 This study was a case-control genome-wide association study of 1616 non-Hispanic white cases and 4683 controls. Under an additive model for the minor allele at each SNP, we identified 19 SNPs, representing 7 chromosomal locations (5p15, 6p24, 7q22, 11p15, 15q14-15, 17q21, and 19p13), with genome-wide significant (P 5x10-8) associations using the discovery samples included in this submission. We genotyped the 19 genome-wide significant SNPs in addition to 178 SNPs with 5x10-8 P-value .0001 and found 4 additional loci (3q26, 4q22, 10q24, and13q34) with genome-wide significant SNPs in the meta-analysis.
Länk
Nyckelord
Versioner (1)
- 2022-12-10 2022-12-10 - Chiara Middel
Rättsinnehavare
David A. Schwartz, MD, University of Colorado, Denver - Aurora, CO, USA
Uppladdad den
10 december 2022
DOI
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Licens
Creative Commons BY 4.0
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dbGaP phs000751 GWAS in Fibrosing Interstitial Lung Disease
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