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 2026-10-29).
Interprets consumer DNA test variants (rsIDs/genes from 23andMe, AncestryDNA) for longevity relevance, providing honest effect sizes, actionability tiers, and myth-busting flags
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.
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.
GEThttps://longevitypulse.theaslangroupllc.com/api/longevity/dna?utm_source=zero.xyzChoose 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.
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
{
"type": "json",
"errors": {
"400": {
"example": {
"error": "invalid request"
},
"description": "Invalid or missing parameter(s). Returned before the payment gate on paid requests, so a malformed call is never charged. JSON body: { error: <what is wrong and how to fix it> } plus usage hints."
},
"402": {
"description": "Payment required — x402 v2 challenge; the accepts array lists scheme, network, and amount. Retry the same request with a PAYMENT-SIGNATURE (v2) or X-PAYMENT (v1) header. Verification is free."
},
"500": {
"example": {
"error": "upstream_failed"
},
"description": "Unexpected server error. If a payment settled without a usable result, contact info@theaslangroupllc.com with the settlement tx hash for a re-run or credit."
}
},
"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"
]
}
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