altar-genomics/clinvar-20260928-hg38

ClinVar 2026-09-28, GRCh38 Per-allele ClinVar records derived from NCBI's dated GRCh38 VCF release clinvar_20260928.vcf.gz (plus the chrY pseudoautosomal file clinvar_20260928_papu.vcf.gz), in the Parquet layout that the Altar altar-clinvar binding reads: 4,555,530 alleles in 26 files. This is a derived copy published by the Altar maintainers, not an NCBI product. The authoritative data is NCBI's release at https://ftp.ncbi.nlm.nih.gov/pub/clinvar/vcf_GRCh38/. How it… See the full description on the dataset page: https://huggingface.co/datasets/altar-genomics/clinvar-20260928-hg38.

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