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        <identifier>oai:figshare.com:article/33752335</identifier>
        <datestamp>2026-09-14T19:11:14Z</datestamp>
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          <dc:title>Human kidney cortex splicing QTL summary statistics</dc:title>
          <dc:creator>samer mohandes (24866764)</dc:creator>
          <dc:subject>Genomics and transcriptomics</dc:subject>
          <dc:subject>splicing QTL</dc:subject>
          <dc:subject>kidney cortex samples</dc:subject>
          <dc:subject>SQTL</dc:subject>
          <dc:subject>Alternative splicing variant</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;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.&lt;/p&gt;&lt;p dir="ltr"&gt;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.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-14T19:11:14Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.6084/m9.figshare.33752335.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Human_kidney_cortex_splicing_QTL_summary_statistics/33752335</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
          <dc:rights>Open Access after 2027-03-14</dc:rights>
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