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Subsets and Splits
ClinVar Pathogenic Variants
Retrieves all records labeled as pathogenic variants from the ClinVar VEP results dataset, providing basic filtering but offering limited analytical insight beyond simple data retrieval.
Random ClinVar VEP Results Sample
Retrieves a sample of variant effect predictions labeled as pathogenic, which helps identify potentially harmful genetic variants but doesn't provide deeper analytical insights.
Random Sample of ClinVar VEP Results
Randomly samples 2000 rows from clinical variant effect predictor results, providing basic dataset exploration but offering no meaningful analytical insights or patterns.