myvariant.variants.batch
shallowio.github.whiteknightonhorse/apibase · Verify this server
Retrieve annotations for up to 1000 genetic variants in a single request by providing a comma-separated list of dbSNP rsIDs or HGVS variant IDs. Returns ClinVar significance, CADD scores, gnomAD allele frequencies, and functional consequence predictions for each variant in one call. Ideal for annotating VCF files, enriching GWAS hit lists, building polygenic risk score pipelines, or bulk pharmacogenomics analysis. Variants not found in the database are marked with found=false. Mix rsIDs from different chromosomes freely — no grouping by position required.
1 trials · measured 28 days ago
myvariant.variants.batch scores 100.0/100 on Vouch's measured behaviour index, from 1 real invocation trials against io.github.whiteknightonhorse/apibase, measured 23 Sept 2026 under methodology v0.2.0. Every measured component scored 100.
Component breakdown
| Component | Weight | Value |
|---|---|---|
| Reliability | 35% | not applicable |
| Schema integrity | 25% | 100.0 |
| Failure behaviour | 15% | not applicable |
| Latency | 15% | not applicable |
| Concurrency | 10% | not applicable |
Tool details
- Transport
- remote + stdio
- Credential class
- self-provisionable
- Input schema
- not declared
- Output schema
- not declared
- Side-effect classification
- unclassified
Score history
| Day | Score | Tier | Methodology |
|---|---|---|---|
| 2026-09-23 | 100.0 | shallow | v0.2.0 |
Probe evidence
| Probe | Outcomes |
|---|---|
| schema_integrity | pass: 1 |
Raw request/response logs are not archived yet — the outcome counts above are drawn directly from every recorded trial.
Embed this score
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[](https://vouch.tools/tools/931f3363-3793-4662-b710-e26ba95d80fb)