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README.md
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# ClinVar VEP
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A ClinVar variant-effect-prediction (VEP) benchmark with two
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Each split is a
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## Subsets
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path: non_coding/*.parquet
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# ClinVar VEP
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A ClinVar variant-effect-prediction (VEP) benchmark, for evaluating DNA language models on clinical variant pathogenicity, with two subsets: **coding** (39,473 variants) and **non-coding** (15,258 variants).
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Each split is a balanced binary classification task: `label = 1` for pathogenic / likely pathogenic and `label = 0` for benign / likely benign.
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## Subsets
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