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metadata
license: apache-2.0
task_categories:
  - text-classification
language:
  - en
tags:
  - dna
  - genomics
  - variant-effect-prediction
  - clinvar
size_categories:
  - 10K<n<100K
configs:
  - config_name: coding
    data_files:
      - split: test
        path: coding/*.parquet
  - config_name: non_coding
    data_files:
      - split: test
        path: non_coding/*.parquet

ClinVar VEP

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).

Each split is a balanced binary classification task: label = 1 for pathogenic / likely pathogenic and label = 0 for benign / likely benign.

Subsets

Config # variants benign pathogenic Region scope
coding 39,473 17,231 22,242 exonic protein-coding
non_coding 15,258 7,629 7,629 intronic + 5′/3′ UTR
from datasets import load_dataset
coding     = load_dataset("hf-carbon/clinvar-vep-final", "coding",     split="test")
non_coding = load_dataset("hf-carbon/clinvar-vep-final", "non_coding", split="test")

Coding subset — origin

For the coding ClinVar benchmark, we use the ClinVar VEP subset from GenerTeam/variant-effect-prediction, which was originally used in the GPN-MSA study (Benegas et al., 2025). However, wee found that it is largely coding: 39,473 are coding and 1,503 are non-coding. The non-coding subset is also highly label-imbalanced, with 10 pathogenic non-coding variants. We therefore use this dataset as our coding ClinVar benchmark and construct a separate balanced non-coding subset from ClinVar.

Non-coding subset — construction

To construct a separate non-coding ClinVar benchmark, we start from the original ClinVar VCF and restrict to single-nucleotide variants on chromosomes 1–22, X, and Y with binary clinical labels, mapping benign / likely benign to label = 0 and pathogenic / likely pathogenic to label = 1. We retain reviewed variants, annotate each variant using ClinVar consequence terms into broad region classes (coding, non_coding, splice, unknown) and finer subtypes (intronic, utr_5_prime, utr_3_prime, etc.), and then select the clean non-coding subset with coding_status == "non_coding".

This yields a balanced non-coding benchmark of 15,258 variants: 7,629 benign and 7,629 pathogenic, covering intronic (10,310) and UTR variants (4,948 total — 4,174 5′UTR + 774 3′UTR).