1To act onBeing written
Is there anything to take to a doctor?
This section stays open until three steps finish. Cancer predisposition is running (22 of about 45 min); the secondary findings and the clinical filter wait on it. Until then this page says nothing either way.
2MedicinesHalf written
Which medicines should a prescriber know about?
New at 12:414 genes with a changed function. HLA typed: none of the listed drug-reaction alleles is present.
The drug list (one row per medicine) is typeset when the guideline lookup runs; it is next in the queue.
3For your familyWritten 12:58
What could be passed on to a child?
New at 12:582 pathogenic changes, one copy each, in recessive genes. A carrier is not affected; it matters if a partner carries the same gene.
4Worth a lookWaiting
Repeats, Lp(a), blood clones, mosaic changes.
Waits on Lp(a), blood clones (CHIP), mosaic changes and mitochondria (running, 4 of about 12 min). Repeats are sized already and join this section when it opens.
5Can I trust this?Written 10:14
About the data, not the person.
Data qualitySex from the reads is XY, as declared. Mean depth 34.1×, 97.8% of the genome at 10× or more. Another person's DNA: 0.2%, below the 3% line. 4,672,118 variants pass, Ti/Tv 2.06.
6OriginsWritten 11:20
Paternal line, maternal line, Neanderthal share and the ancestry projection are in. The finer regional split waits on its own step.
7Traits and scoresBeing written
Traits, blood groups, and risk scores with an ancestry-matched percentile.
Traits and blood groups are in. Scores are computing now (9 of about 55 min); a score appears only with its matched percentile.
8Assessed, no findingAt the end
Each step with nothing to report still says what it looked at.