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Copy file name to clipboardExpand all lines: src/components/table/EqtlTableDescription.vue
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<li><strong>phenotype_id:</strong> gene identifier affected by eQTL</li>
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<li><strong>variant_id:</strong> genetic variant, in format <code>{chromosome}_{position}_{ref}_{alt}</code></li>
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<li><strong>pip:</strong> SuSiE posterior inclusion probability. Essentially, the probability the variant is a causal one for this eQTL signal</li>
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<li><strong>cs_id:</strong> Credible set identfier within a tissue and phenotype. The cs_id together with the tissue and phenotype_id (Ensembl id) uniquely identify a credible set. A credible set containing more than one genetic variant will have multiple records.</li>
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<li><strong>cs_id:</strong> Credible set identifier within a tissue and phenotype. The cs_id together with the tissue and phenotype_id (Ensembl id) uniquely identify a credible set. A credible set containing more than one genetic variant will have multiple records.</li>
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