Prader-Willi/Angelman Syndrome, DNA Methylation Analysis

Understand what Prader-Willi/Angelman Syndrome, DNA Methylation Analysis signals

LOINC codes: 41117-3
Commercial laboratory assays: 1

We have not added a physiological summary for this biomarker yet. Compare the commercial laboratory assays and population reference ranges below.

Compare commercial laboratory assays for Prader-Willi/Angelman Syndrome, DNA Methylation Analysis

Check orderable catalog codes, specimen types, fasting requirements, and demographic reference ranges across laboratories.

Prader-Willi/Angelman Syndrome, DNA Methylation Analysis

Laboratory: Quest Diagnostics
Test code: 11369
Specimen: Blood
Fasting: Not stated
LOINC: 41117-3
Turnaround: Set up: Wed

Laboratory assay overview

This test will detect Prader-Willi or Angelman syndrome in a patient with clinical suspicion of either of these disorders. The test detects methylation changes in the chromosome 15 q11-13 region that are responsible for more than 99% of PWS and about 80% of AS.

View complete laboratory reference notes

See Laboratory Report

Quest Diagnostics test directory, test code 11369

Verify these ranges and sources

We compile every detail above directly from named laboratory directories and published clinical studies. Laboratories calculate standard reference intervals from the statistical distribution of tested populations for a specific assay method and demographic group, rather than setting universal optimal targets.

Always review your personal lab results with a licensed clinician, or track your lab history and health goals in Aumnivida.

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