Provenance record

AlphaGenome Atlas: A predictive map of every possible DNA letter change in the human genome

Google DeepMind (tier 1, lab) 2026-09-08T14:00:15.000Z Original ↗

Source note: Primary statements from a frontier lab.


Discourse valence
+7
Mixed or uncertain
confidence 74% · 5 items · range -100 to +75
Adverse readingFavourable reading
Consensus of 5 models from different labs. Spread 175 points, agreement low.
AGI and timelinesBiological and chemical upliftExistential and catastrophic risk
Excerpt as ingested

AlphaGenome Atlas maps the molecular effects of 9 billion single-letter DNA variants across the human genome.

Every model that read this

ModelProviderStageScoreConf.LatencyPromptWhen
Llama 3.3 70BMetaanalysis 0 70%4525ms v1.0.0 / m1.0.1 2026-09-10 09:18
GPT-4.1 miniOpenAIconsensus +25 80%2542ms v1.0.0 / m1.0.1 2026-09-10 12:19
Claude Sonnet 5Anthropicconsensus +35 40%7558ms v1.0.0 / m1.0.1 2026-09-10 12:19
Gemini 2.5 FlashGoogleconsensus -100 90%2845ms v1.0.0 / m1.0.1 2026-09-10 12:19
Mistral Small 3.1 24BMistral AIconsensus +75 90%4516ms v1.0.0 / m1.0.1 2026-09-10 12:19
Llama 3.3 70B · reading

Maps DNA variants

evidence: primary horizon: n/a
GPT-4.1 mini · reading

Mapping the effects of every possible DNA letter change could significantly enhance genetic research and medicine, potentially improving disease understanding and treatment. However, the societal impact depends on how this information is applied, including privacy concerns and ethical issues, which introduces mixed implications.

evidence: primary horizon: near capability 70 societal 30 existential 5 economic 40
Claude Sonnet 5 · reading

This is a genuine scientific tool release with plausible medical research benefits, but the text gives no evidence of validation, adoption, or downstream impact. The implication for human flourishing is positive but currently speculative, resting only on the tool's existence and stated scope.

evidence: reported horizon: n/a
Gemini 2.5 Flash · reading

AlphaGenome Atlas provides a comprehensive map of DNA variants and their molecular effects. This tool significantly advances genomic understanding, enabling better disease prediction, diagnosis, and treatment. The primary implication is a positive impact on human health and scientific research.

evidence: reported horizon: n/a
Mistral Small 3.1 24B · reading

The mapping of 9 billion single-letter DNA variants provides extensive data on genetic variations. This can lead to significant advances in personalized medicine and genetic research.

evidence: primary horizon: n/a existential 0

Evidence extracted

The chain
SOURCE     Google DeepMind (tier 1)
   ↓
DOCUMENT   b73686f8-0b48-4e33-b94c-559c7ebe6fcc
           https://deepmind.google/blog/alphagenome-atlas-a-predictive-map-of-every-possible-dna-letter-change-in-the-human-genome
   ↓
EVIDENCE   1 extracted excerpt
   ↓
MODEL RUN  5 runs, methodology 1.0.1
   ↓
SCORE      +7  (Mixed or uncertain)
   ↓
CONFIDENCE 74%