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This is the real product. Scroll it, search it, check its sources.

Everything below is the actual interface — the same Dashboard, Explorer, search, evidence trail, and exports you'll get — generated from an anonymous, public-source genome. No real person is identified. Your report will be built from your own DNA file.

642,089
SNPs scanned
238
Annotated SNPs analyzed
15
Categories with findings
10
Public databases checked
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Two views of the same genome

The Dashboard summarizes your interpreted genetics as the science evolves; the Explorer is where you investigate it. Both are fully live below — search, filter, follow, and export all work.

Sample dashboard. A fully interactive replica built on an illustrative genome — search, filter, follow, and export all work right here. Private notes, doctor reports, and monitoring live in your own account.
Knowledge GC-2026.09.06
Report v2
Current

Your Genetic Dashboard

Your DNA doesn’t change. Our understanding of it does.Synchronized with knowledge GC-2026.09.06.

anonymous-sample-genome.txt · rendered live from knowledge GC-2026.09.06 — interpretations are referenced from our research library, never copied.

····

Since Your Last Visit

New 2Expanded 11 followed variant affected1 Saved View affected
expandedrs1801133MTHFR2026-10-15

Two additional population studies were added supporting the mild, diet-modifiable effect of the C677T variant on folate metabolism.

newrs4149056SLCO1B12026-10-06

A CPIC guideline revision strengthened the dosing recommendation around simvastatin for SLCO1B1 C-allele carriers.

newrs1041981ADH1B2026-10-08

New public research about ADH1B was folded into this interpretation.

Nothing is ever changed automatically: if newer research affects a doctor report or export you shared, it is flagged in For My Doctor and Export History.

Variants Monitored
238
SNPs retained in your pseudonymous index
Interpreted Findings
238
+4 vs. previous snapshot
Insight Categories
15
Areas of your genetics with interpretations
Evidence Sources
10
Public databases contributing to your report

Profile at a Glance

238findings
Strong
Moderate
Limited

Dashboard Freshness

Research Pending
Knowledge GC-2026.09.06

3 of your findings are awaiting fuller research coverage — a normal part of ongoing science, not a concern.

3 findings in fuller research
“Current” means synchronized to the latest completed knowledge — some questions are simply still being researched.
2 findings awaiting audit
Independent verification passes re-check annotations over time — part of how we stay accurate.

Report tracking decides which of your reports participate in monitoring — it works alongside your monitoring subscription, never instead of it.

Featured Discovery
Pharma
Strong evidence
Stable interpretation
SLCO1B1
TT

SLCO1B1 variant (rs4149056)

The C allele of SLCO1B1 increases the risk of muscle pain (myopathy) when taking the statin simvastatin. Discuss statin choice with your clinician. Your genotype for rs4149056 is TT.

Explore this finding

Explore Your Genetics

Go deeper than the summary: investigate your variants, genes, categories, and the public evidence behind every interpretation in the research library.

Open Explorer

Saved Views

Following

  • rs1801133MTHFR · MTHFR variant (rs1801133)1 updateMonitoring
  • rs4149056SLCO1B1 · SLCO1B1 variant (rs4149056)1 updateMonitoring
  • rs1041981ADH1B · Your Alcohol Processing Speed1 updateMonitoring

Following is your personal watchlist — it never changes how findings are ranked or interpreted.

Export History

1 with newer intelligence
  • My Genetic Dashboard — Sep 2026Dashboard · PDFOct 18, 2026Knowledge GC-2026.09.06Report v212 findings
  • Strong pharmacogenomics viewGenetic Explorer · HTMLOct 22, 2026Knowledge GC-2026.09.062 findings
    Newer Intelligence Available1 finding with newer interpretationsas of Oct 25, 2026, 4:39 PM
  • Doctor visit — Dr. AlvarezFor My Doctor · PDFSep 27, 2026Knowledge GC-2026.09.06Doctor v13 findings

Exports stay in your history for as long as your account exists — even after monitoring is canceled.

Your Genetic Journey

  1. First analysis2026-06-08
  2. Monitoring active since2026-06-09
  3. Reports generated1
  4. Report snapshots1 version · latest 238 findings
  5. Knowledge updates presented15
  6. Variants you follow3
View Full History

Suggested for You

Based only on your own activity and preferences — never on hidden scores, and never changing how findings are evaluated.

  • New research is relevant to a variant in your DNA
    rs1801133MTHFR

    Two additional population studies were added supporting the mild, diet-modifiable effect of the C677T variant on folate metabolism.

  • New research is relevant to a variant in your DNA
    rs4149056SLCO1B1

    A CPIC guideline revision strengthened the dosing recommendation around simvastatin for SLCO1B1 C-allele carriers.

  • New research is relevant to a variant in your DNA
    rs1041981ADH1B

    New public research about ADH1B was folded into this interpretation.

Fun Fact 1 of 25

Your Alcohol Processing Speed

With your CC genotype, your body processes alcohol at its own unique pace, which is a key player in how you experience your favorite beverage.

rs1041981 · ADH1B · CC

Educational information only. Not medical advice — these associations describe population statistics, not individual predictions.

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