Every number on this page is read from the database as you load it — nothing here is a marketing figure typed in by hand. The catalog grows on its own schedule, gets fact-checked against primary sources, and is free for anyone to reuse.
New findings are pulled from the public GWAS Catalog six times a day and published only if they pass a fixed quality gate. The curve is the running total; the bars underneath are what landed each day.
Three things run whether or not anyone is watching, and the results — including the unflattering ones — are shown below.
New associations are imported from the GWAS Catalog six times a day. Anything whose underlying allele data isn't clean is refused rather than guessed at.
Every cited PMID is checked against Europe PMC for matching author and title, every source URL for reachability, and every MONDO/ICD-10 code against its registry. Mismatches are flagged, not published.
A nightly watch flags pages whose linked variants have picked up newer research, and pages that have gone too long without a fact-check.
TAS2R38 · rs10246939 · added Sep 5
See detailed info → StandardTAS2R38 · rs1726866 · added Sep 5
See detailed info → StandardLSP1 · rs907611 · added Sep 5
See detailed info → StandardDBH · rs3025343 · added Sep 5
See detailed info → StandardEXOC3 · rs11739663 · added Sep 5
See detailed info → StandardPUS10 · rs7608910 · added Sep 5
See detailed info →Both datasets are free to take — no key, no signup, no negotiation. Most comparable sources are non-commercial, academic-license-only, or require an approved account; ours is CC BY 4.0, which means you can build on it, publish with it, and ship products on it as long as you credit us.
curl https://www.mygenelog.com/api/v1/variants
All 62 in one response, with per-genotype interpretations and the source cited for each.
curl https://www.mygenelog.com/api/v1/conditions
Linked variants, MONDO/OMIM/ICD-10 cross-references, pharmacogenomic notes, every cited source, the fact-check date — and the open questions we could not resolve.
If you use this in a paper, a thesis, or a product, cite it like any other data source:
MyGeneLog (2026). MyGeneLog variant and condition dataset [Data set]. narubox, Austin, TX. Retrieved from https://www.mygenelog.com/data
@misc{mygenelog,
title = {MyGeneLog variant and condition dataset},
author = ,
year = {2026},
note = {CC BY 4.0},
url = {https://www.mygenelog.com/data}
}
Working on something research-grade and need a versioned snapshot, a bulk export, or a field we don't expose yet? Ask us — we would rather build it than have you scrape it.
The edges, not the nodes. Variant catalogues, disease ontologies, pharmacogenomic guidelines and chemosensory research each already exist as excellent open resources, and each is separate from the others. Here every variant carries the conditions it links to, every condition carries the gene-drug pairs that apply, the drug pages read the same pharmacogenomics from the other direction, and smell and taste sit alongside them because they are how food gets chosen in the first place. Anyone can rebuild our node lists from public sources; the joins are what took the work.
Yes. Condition pages are licensed CC BY 4.0, which permits commercial reuse with attribution to MyGeneLog. This is deliberate: most comparable sources are non-commercial-only, academic-license-only, or require an approved account, which blocks exactly the people who would build something useful.
No. Both /api/v1/variants and /api/v1/conditions are open, unauthenticated JSON endpoints. A light rate limit applies (10 requests per minute per IP) because this runs on a small server, not a CDN. If you need more, ask and we will work something out rather than have you scrape.
Variants are collected from the public GWAS Catalog six times a day and published only if they pass a fixed quality gate. Condition pages are written and fact-checked individually, then re-checked on a schedule; each carries the date of its last verification. Citations and identifier codes are re-validated weekly against Europe PMC, MONDO and the ICD-10 registry.
In two passes. A deterministic script confirms every cited PMID matches its stated author and title, that every source URL resolves, and that every MONDO/ICD-10 code denotes the entity claimed. Then a separate reviewer that did not write the page re-checks the claims against primary sources for meaning, framing and missing caveats. Both have caught real errors, which is why both exist.
Because a dataset that only shows its strengths is harder to trust, not easier. Where we could not source a figure, where an identifier does not exist yet, or where a guideline is behind a paywall, we record it and expose it through the API alongside the content. You should be able to see the edges of what we verified.
The list endpoints already return the full dataset in one response, so no pagination is needed. If you need a frozen, citable snapshot for a paper — or a field we do not currently expose — get in touch and we will produce it.
Licensed CC BY 4.0. Reuse it, including commercially, with attribution to MyGeneLog. Full API docs →