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ggd-genomics / packages / hg38-clinically-associated-variants-ensembl-v1

All known clinically associated variants at the time of Ensembl release 99. Any variant in ClinVar classified as probably/likely-pathogenic, pathogenic, drug-response, or histocompatibility are included. Decomposed and Normalized. Remapped from Ensembl GRCh38 to UCSC hg19. Ensembl variant info page can be found at: https://uswest.ensembl.org/info/genome/variation/index.html

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