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LongevityPulse DNA Variant Interpreter
x402
LongevityPulse DNA Variant Interpreter is a paid API for AI agents from longevitypulse.theaslangroupllc.com, paid per call via x402, $0.2/call, status unknown (last checked 2026-09-15).
Interprets consumer DNA test variants (rsIDs/genes from 23andMe, AncestryDNA) for longevity relevance, providing honest effect sizes, actionability tiers, and myth-busting flags
Price / call$0.2
Success—
StatusUnknown
How this service works
DNA variant interpretation for longevity agents. Reads consumer-test genes/rsIDs (23andMe, AncestryDNA) e.g. APOE-e4, MTHFR-C677T, FOXO3. Honest effect sizes (not fear), actionability tiers, myth-flags overstated claims like MTHFR panic, and says plainly when a variant lacks real evidence. Not medical advice.
Output
Returns a structured interpretation of the queried DNA variant including: honest effect size (not sensationalized), actionability tier indicating how much the variant should influence behavior, a myth-flag if the variant is commonly overstated in popular media, evidence quality rating, and a plain-language summary of what the variant actually means for longevity — with a clear disclaimer that this is not medical advice.
Example use cases
Evaluate genetic risk for cognitive aging
“I have the APOE-e4 variant from my AncestryDNA test — how much should I actually worry about this for my brain health as I age, and what can I realistically do about it?”
Debunk health supplement hype claims
“A lot of wellness brands claim I need special supplements because I'm MTHFR C677T positive — is that panic justified by actual science, or am I being sold something I don't need?”
Prioritize actionable genetic findings
“My 23andMe results show several longevity-related variants like FOXO3 and APOE — which ones are worth actually changing my behavior for, and which are just interesting but not actionable?”
Technical details
Endpoint
GEThttps://longevitypulse.theaslangroupllc.com/api/longevity/dnaWhen to prefer
Choose this endpoint when an agent needs to interpret specific consumer DNA test results (23andMe, AncestryDNA) for longevity context, especially when honest calibration of effect sizes and myth-busting of overhyped variants like MTHFR is important. Prefer this over generic medical databases when the user has actual rsID or gene-name inputs from a consumer test and wants actionable, evidence-tiered longevity guidance rather than raw clinical data.
Side effects
- Unknown or unsupported rsID returns no interpretation with a notice that the variant lacks evidence
- Malformed gene/rsID input returns a validation error
- Variant exists in database but has insufficient longevity-specific evidence — returns low-evidence flag rather than interpretation
- Rate limiting or payment failure returns 402 Payment Required
- Overly broad query without a specific variant returns a prompt for a specific rsID or gene name
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Output
Schema · Response
{
"type": "json",
"example": {
"results": [
{
"gene": "APOE",
"input": "APOE-e4",
"recognized": true,
"effect_size": "One ε4 copy: ~2-3x Alzheimer's odds ratio vs ε3/ε3; two copies: ~8-12x — one of the largest common-variant effect sizes in human genetics, still a probabilistic shift, not a diagnosis",
"actionability_tier": "well-replicated",
"resolved_identifier": "rs429358 (APOE ε4 tagging SNP)"
},
{
"input": "MTHFR-C677T",
"myth_flag": {
"the_myth": "Marketed as a serious \"detox\"/methylation defect requiring supplement protocols",
"is_commonly_overstated_or_mythologized": true
}
}
],
"variants_requested": [
"APOE-e4",
"MTHFR-C677T",
"FOXO3"
]
}
}Tags
x402
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