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Additional file 7 of Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes

Year: 2021

Type: dataset

Abstract: Additional file 7: Table S6. Comparison of association results to independent data. For each gene-trait pair, we list the original p-value, the GWAS trait(s) that we classified as most similar to a PheWAS trait, its best p-value in an independent dataset, the number of GWAS datasets that were used for this trait, and the rank of this gene within that dataset. For UK Biobank summary statistics, we have genome-wide data; for datasets with individual-level data, only 16p11.2 and 22q11.2 genes were calculated. See Table S2 for more information on datasets used.

Source: Figshare

DOI: 10.6084/m9.figshare.16907212

Authors: Vysotskiy, Mikhail, Zhong, Xue, Miller-Fleming, Tyne W., Zhou, Dan, Cox, Nancy J., Weiss, Lauren A.

Institutions: University of California, San Francisco, Vanderbilt University Medical Center

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W4394444837

Cites: 97

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Related to: 10