Genomic Unity® MECP2 Gene Analysis
Genomic Unity® MECP2 Gene Analysis is an effective test for the genetic cause of Rett syndrome, atypical Rett syndrome and/or learning disabilities.
For comprehensive coverage of learning disability and intellectual disability-related genes in addition to MECP2, consider Genomic Unity® Intellectual Disability Analysis.
Order this test when the patient presents with symptoms of Rett syndrome, atypical Rett syndrome and/or learning disabilities, and you'd like the option to reflex up to Genomic Unity® Whole Genome Analysis.
- Sequencing analysis of the MECP2 gene
- Del/dup analysis of the MECP2 gene
Optionally includes:
- Reflex to Genomic Unity® Whole Genome Analysis or Genomic Unity® Exome Analysis
MECP2
SNVs and Indels up to 50bp
99.7% sensitivity
99.6% positive predictive value
Structural variants:
96% clinical sensitivity
81302, 81304, 81479
The CPT codes provided are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
Blood - 5ml
Saliva - contact us for a kit
gDNA - 5μg