Update to DeepDNA
Snapshot Nov 9, 2026 · 01:25 UTC · version 1.3.1
Product listing or positioning changed
Full description — Now says: Cited pharmacogenomics: drug–gene records, most from CPIC and DPWG guidelines, plus gene and rsID lookups and a medication list screen. Read-only; takes no...
Observed in the public listing; claims come from the publisher.
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Full description
Nov 7, 2026 · 13:29 UTC
Cited pharmacogenomics: CPIC and DPWG drug–gene guidance, gene and rsID lookups, and a medication list screen. Read-only; takes no genotype or DNA file.
Nov 9, 2026 · 01:25 UTC
Cited pharmacogenomics: drug–gene records, most from CPIC and DPWG guidelines, plus gene and rsID lookups and a medication list screen. Read-only; takes no genotype or DNA file.
Long description
Nov 7, 2026 · 13:29 UTC
generic drug names into drugs with a curated drug–gene record and drugs not covered, and says whether each record rests on a CPIC or DPWG guideline, a drug label or the primary literature. - lookup_drug_gene: guidance for a gene, or for ...
Nov 9, 2026 · 01:25 UTC
up to 30 generic drug names into drugs with a curated drug–gene record and drugs not covered, and says whether each record rests on a CPIC or DPWG guideline, a drug label or the primary literature. - lookup_drug_gene: the record for a ge...
Short description
Nov 7, 2026 · 13:29 UTC
Cited drug-gene guidance
Nov 9, 2026 · 01:25 UTC
Cited drug-gene records
Composer icon url
Nov 7, 2026 · 13:29 UTC
https://files.openai.com/content?id=file_00000000cffc8243a30dfc054569a826
Nov 9, 2026 · 01:25 UTC
https://files.openai.com/content?id=file_000000006c188243a49de88ec9600a91
Compare saved observations
Download comparison JSONFull technical diff · 7 changed fields
changed /release/description
"Cited pharmacogenomics: CPIC and DPWG drug–gene guidance, gene and rsID lookups, and a medication list screen. Read-only; takes no genotype or DNA file."
"Cited pharmacogenomics: drug–gene records, most from CPIC and DPWG guidelines, plus gene and rsID lookups and a medication list screen. Read-only; takes no genotype or DNA file."
changed /release/id
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changed /release/interface/logo_url
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changed /release/interface/long_description
"DeepDNA gives ChatGPT curated, cited records on pharmacogenomics, so answers about a gene, a variant or a drug–gene pair can quote their sources.\n\nFive read-only tools:\n- check_medications: splits a list of generic drug names into drugs with a curated drug–gene record and drugs not covered, and says whether each record rests on a CPIC or DPWG guideline, a drug label or the primary literature.\n- lookup_drug_gene: guidance for a gene, or for one gene and one drug: the guideline where one exists, the phenotype groups it distinguishes, a summary and sources.\n- lookup_gene: everything curated about a gene, including what a consumer genotyping array can and cannot tell you about it.\n- lookup_variant: one variant by dbSNP rsID, with its gene, alleles on the plus strand of GRCh37, effect and sources.\n- list_genes: what the knowledge base covers.\n\nCoverage is small and reviewed: 12 genes (CYP2C19, CYP2C9, CYP2D6, SLCO1B1, VKORC1, UGT1A1, G6PD, MTHFR, COMT, HFE, APOE, BRCA1) and 51 drug–gene pairs across 11 of them; 40 cite a CPIC or DPWG guideline. A drug that is not covered is reported as not covered, which does not mean it has no pharmacogenomic interaction.\n\nWhat it does not do: it takes no genotype or DNA file (the tools have no field for one), and it never gives a metabolizer status, a diagnosis or a dose. Every response carries the same notice: educational information only, not medical advice. Decisions about a medication stay with the prescriber.\n\nNo account and no key. Requests are counted without IP addresses or request bodies; see the privacy policy."
"DeepDNA gives ChatGPT curated, cited records on pharmacogenomics, so answers about a gene, a variant or a drug–gene pair can quote their sources.\n\nFive read-only tools:\n- check_medications: splits a list of up to 30 generic drug names into drugs with a curated drug–gene record and drugs not covered, and says whether each record rests on a CPIC or DPWG guideline, a drug label or the primary literature.\n- lookup_drug_gene: the record for a gene, or for one gene and one drug, with the guideline where one exists, any phenotype groups it distinguishes, a summary and sources.\n- lookup_gene: everything curated about a gene, including what a consumer genotyping array can and cannot tell you about it.\n- lookup_variant: one variant by dbSNP rsID, with its gene, alleles, effect and sources.\n- list_genes: what the knowledge base covers.\n\nCoverage is small: 16 genes (CYP2C19, CYP2C9, CYP2D6, CYP3A5, DPYD, TPMT, NUDT15, SLCO1B1, VKORC1, UGT1A1, G6PD, MTHFR, COMT, HFE, APOE, BRCA1) and 83 drug–gene pairs across 15 of them; 72 rest on a CPIC or DPWG guideline. A drug that is not covered is reported as not covered, which does not mean it has no pharmacogenomic interaction.\n\nWhat it does not do: it takes no genotype or DNA file (the tools have no field for one). Records report what a guideline, a drug label or the primary literature says, which can include dose adjustments by phenotype; the tools do not work out a metabolizer status or a dose for a person, and they give no diagnosis. Answers are written by ChatGPT, an AI model, using these records. Every record comes with the same notice: educational information only, not medical advice. Decisions about a medication stay with the prescriber.\n\nNo account and no key. We do not store IP addresses, request bodies or medication lists. Each request records the tool, the gene, rsID or drug looked up (for a medication screen, only how many drugs), the client and a country code; see the privacy policy."
changed /release/interface/short_description
"Cited drug-gene guidance"
"Cited drug-gene records"
changed /release/version
"1.3.0"
"1.3.1"
Full snapshot data
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