Eunjung Kim· F · 28

Top of report

Actionable findings

The eight findings below have strong evidence, real-world implications, and would change a doctor's prescribing or screening decisions. Click any card to jump to the full detail.

Pharmacogenomics

Drugs to flag

Findings derived using dbSNP forward-strand convention against CPIC Level A guidelines. These do not change with future re-runs. Photograph for your phone's medical info.

Cardiovascular risk

Cardiology

9p21 risk haplotype is the strongest single-locus CAD signal in your data. Combined with a maternal-grandfather history of heart disease and a borderline-pro-inflammatory cytokine profile, this section warrants the most attention.

Recessive disease carrier status

Carrier

Findings here are asymptomatic in you. Relevance is for family planning — partner screening ($300–400) gives a clean answer for ~280 recessive diseases including the BCKDHA finding below.

Nutrition & metabolism

Nutrition

Curated panel of nutrigenomic SNPs verified against dbSNP forward strand. The MTHFR and vitamin D findings are immediately actionable; the others inform supplementation choices.

Behavior, exercise, sleep

Lifestyle

Variants that don't determine disease but inform how you respond to alcohol, caffeine, training type, salt, and sleep cues.

Polygenic risk scores

PRS

Weighted sums across 18.6 million SNPs from 10 PGS Catalog scoring files. Direction is interpretable; precise percentiles require ancestry-matched reference distributions. Hover a marker on the chart to highlight a trait; click to jump to the detail card.

Per-trait detail

Protocol — derived from findings

Protocol

Each item below is a recommendation generated from one or more findings above. Tier A = strong evidence + direct genotype-driven rationale. Tier B = good evidence, moderate driver. Tier C = emerging / mechanistic.

Supplementation

Lifestyle

Genotype × medical record

Clinical convergences

Where a genetic prediction matches a lab value or documented clinical event, confidence in the finding is reinforced. Below are the strongest convergences from your record.

Lab values (recent encounters)

Next PCP visit agenda

Tap to check off as you discuss / complete each item. Saved locally in your browser.

Common alleles you don't carry

Reassuring

What's not in your data matters too. None of these absences are guarantees, but they're specific high-impact alleles that aren't in play for you.

What this analysis can't tell you

Limits

A 23andMe chip + imputation handles common variants well but is blind to several classes of clinically important variation. If any of the categories below become relevant via family history or symptoms, get a clinical-grade test for that question.