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- # ClinVar VEP — coding + non-coding benchmark
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- A ClinVar variant-effect-prediction (VEP) benchmark with two complementary subsets **coding** (39,473 variants) and **non-coding** (15,258 variants) — for evaluating DNA language models on clinical variant pathogenicity.
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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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+ # 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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