Pricing

A monthly subscription, not a one-time test.

Annual plans are 17% cheaper. No contracts. After cancellation, your data stays accessible read-only for 30 days, then is deleted unless you ask us to retain it.

Most popular

Helica Standard

$29/ month

$24/mo billed annually

  • ·Full PGx panel — every CPIC level A/B gene
  • ·Carrier status (common variants)
  • ·~70 trait calls and basic polygenic risk panels
  • ·Unlimited conversational chat, fully cited
  • ·Quarterly reanalysis with diff alerts
Start Standard

14-day money-back on first paid month. Cancel anytime.

Other plans

Three more, for different needs.

Free

$0always

Best for · Curious 23andMe / Ancestry users

A first taste of Helica — upload a chip-array file and see what's there.

  • ·Ancestry breakdown
  • ·5 trait calls
  • ·2 pharmacogenomic findings
  • ·Read-only chat (3 questions/day)

Clinical

$59/ month

Best for · Customers with whole-genome data

Full WGS depth: structural variants, HLA, full PRS, and the PCP handoff PDF.

  • ·Everything in Standard
  • ·Structural variants (AnnotSV) with credibility tiers
  • ·HLA fine-typing at 4-digit resolution (T1K)
  • ·Full polygenic risk panel (peer-reviewed only)
  • ·Rare-variant carrier screening (ACMG SF v3.2+)
  • ·Unlimited PCP handoff PDFs

Family

$79/ month

Best for · Couples planning, multi-genome households

Up to five genomes. Cross-household carrier matching. De novo P/LP alerts.

  • ·Everything in Clinical
  • ·Up to 5 genomes per household
  • ·Autosomal-recessive carrier matching across genomes
  • ·De novo P/LP variant alerts
  • ·Family-tree variant inheritance view

Full comparison

Everything, in a single table.

FeatureFreeStandardClinicalFamily

Data sources

Chip-array files (23andMe, Ancestry, MyHeritage)
Whole-genome files (VCF, BAM, CRAM)
Multiple genomes per account1115

Findings

Ancestry
Trait calls5~70~70~70
Pharmacogenomics (PGx)2 findingsFull panelFull panelFull panel
Common-variant carrier status
Rare-variant carrier (ACMG SF)
Structural variants (AnnotSV, credibility-tiered)
HLA fine-typing (T1K, 4-digit)
Polygenic risk (peer-reviewed only)BasicFullFull
Cross-household carrier matching

Experience

Conversational chat (cited)3 q/dayUnlimitedUnlimitedUnlimited
Quarterly reanalysis with diff alerts
PCP handoff PDFUnlimited5 / mo
Clinician review add-on (partner-dependent — pricing TBD)

Coming late 2026

Helica Clinical — sequencing kit + 12 months.

A spit-kit through a CLIA-certified wet-lab partner, paired with twelve months of the Clinical tier. Designed for customers who want full-depth findings without choosing a sequencing provider first.

$499

Spit-kit + 12 months Clinical

Join waitlist

What we won’t do

This list matters as much as the feature list.

  • Embryo screening or PGT-P.

    Permanently. We don't interpret embryos, fetal samples, or any prenatal genetic data. We will not partner with companies that do.

  • Longevity hand-waving.

    When we can cite a peer-reviewed validated score, we'll ship it. Until then, we leave the longevity narrative to the supplement market.

  • Telling you what to take.

    We never recommend a drug, dose, supplement, or treatment plan. Findings are informational. Clinical decisions are between you and your prescriber.

  • Selling your data.

    We don't share, rent, or sell genetic data to researchers, pharmaceutical companies, or advertisers without your explicit, granular, revocable opt-in.

Free tier

Try it before you pay for it.

Upload a 23andMe or Ancestry file. See two real PGx findings on your own genome. Upgrade only if it's useful.

All prices in USD. Annual plans billed up-front at a 17% discount. Helica is informational and not a substitute for medical advice. Discuss any change to your medications with a licensed prescriber.