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Human kidney cortex splicing QTL summary statistics

Year: 2026

Type: dataset

Abstract: This dataset contains kidney cortex splicing quantitative trait locus (sQTL) summary statistics from 404 human nephrectomy samples. The file includes SNP-splicing phenotype associations for significant intron clusters, filtered to retain associations where the nominal p value is less than or equal to the cluster-level q value. Genomic coordinates are based on hg19.Each row represents one SNP-splicing phenotype association. The splicing phenotype identifier includes chromosome, start, end, intron cluster ID, strand, and Ensembl gene ID. The file includes variant position, variant ID, phenotype ID, effect size, standard error, nominal p value, sample size, gene ID, and gene name.

Source: Figshare

DOI: 10.6084/m9.figshare.33752335

Author: samer mohandes

Topic: RNA Research and Splicing

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funder: National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G1001445874, G2503904646, G42520651, The role of cytosolic nucleotide sensors in inflammatory fibrosis

OpenAlex ID: W7212714636

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