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IndiPGx-Pop p092

Lab reportcohort · india-sim

10/30/2026, 1:55:19 PM · PharmCAT 3.4.0 · Research record, not medical advice

6
Genes standardised
6
Calls quoted
0
Coverage gaps
0
Identifiers removed
29.4s
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  1. Muse Sparkread 6 gene calls18.4s
  2. PharmCATstandardised 6 genes11.0s
  3. Rules0 coverage gaps

CallsMuse Spark each call quoted from the source, then standardised by PharmCAT

Synthetic Genomics Lab (Kochi) · 20 Oct 2026 · open original photo

Uploaded lab report photo
GeneAs printedStandardisedPhenotype term
CYP2C19“*3/*1 | Intermediate metabolizer”*3/*1Intermediate Metabolizer
CYP2D6“*10/*1 | Normal metabolizer (activity score 1.25)”*10/*1Normal Metabolizer · activity 1.25
DPYD“No tested variant detected | Normal metabolizer (activity score 2)”Reference/ReferenceNormal Metabolizer · activity 2.0
NUDT15“*1/*1 | Normal metabolizer”*1/*1Normal Metabolizer
TPMT“*1/*1 | Normal metabolizer”*1/*1Normal Metabolizer
UGT1A1“*28/*1 (TA7/TA6) | Intermediate metabolizer”*28/*1Intermediate Metabolizer

Method as printed: Method: targeted genotyping by real-time PCR. Only the listed variants are assayed; variants outside this panel cannot be excluded.

Coveragedeterministic rules · which India-relevant variants this panel named

DPYDHapB3named on the report

Most common Indian decreased-function DPYD variant (~3.3%, PMID 40810747)

DPYDc.85T>C (*9A)named on the report

~25% in Indians; toxicity signal in South Indian cohorts (PMC11300675)

DPYD*2Anamed on the report

European tier-1 variant; rare in Indians (PMID 40810747)

DPYD*13named on the report

Tier-1 no-function variant (PMID 39032821)

DPYDc.2846A>Tnamed on the report

Tier-1 variant; near-absent in Indians (PMID 40810747)

NUDT15*3named on the report

Main NUDT15 risk allele, ~7-11% in Indians (PMID 29470173)

UGT1A1*28named on the report

TA-repeat allele, common in South Asians

UGT1A1*6named on the report

East Asian allele; reported at low frequency in India

TPMT*3Cnamed on the report

Most common TPMT variant in South Asians

CYP2C19*2named on the report

Common no-function allele in South Asians

CYP2C19*17named on the report

Increased-function allele

A variant the panel did not name is left out of cohort statistics for that variant, rather than counted as absent. Reader notes: Only the listed variants are assayed; variants outside this panel cannot be excluded. Synthetic document generated for software benchmarking. Not a real patient or laboratory.

Exportde-identified · the same record in three formats

Curator review

A curator checks each call against the source document before the record counts in a cohort, and Muse Spark web search finds published Indian frequency data for each variant. Both are written to the audit log. Reviewing is the one action that needs a curator code, because it is a claim that a person checked the page.

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Research tool, not medical advice. Pathya reads and standardises pharmacogenomic results; it makes no dose, drug or test recommendation. Audit log: data/cases/bdacf5793cc5/audit.log.