Comprehensive Lipidemia Panel
A 27-gene panel for assessing hereditary lipidemia, powered by the Helix Exome+® platform for comprehensive lipid disorder evaluation.
Turnaround
6-21 days
Requery (SOQO)
≤ 5 days
Genes Tested
27
Panel Description
This panel evaluates 27 genes associated with hereditary lipidemia.
Order This Test
Contact our clinical team to order this panel or learn more.
Indications for Testing
A relevant personal and/or family history suggestive of hereditary lipidemia.
Methodology
This test utilizes next-generation sequencing to detect single nucleotide variants, insertions and deletions up to 20 bp, and copy number variants in genes associated with a variety of hereditary lipidemia conditions.
Technical Specifications
Analytical sensitivity (SNV)
> 99%
Analytical sensitivity (indel)
> 99%
Analytical specificity
> 99%
CNV sensitivity (multi-exon)
> 99%
CNV sensitivity (single-exon)
> 90%
Gene notes
ABCA1: Evaluation of exon 40 will not be performed. SAR1B: Sensitivity in exon 4 may be reduced.
Genomic build
GRCh38
Genes Tested
27 genes included in this panel
Ordering Information
Turnaround Time
Typically 6-21 days (standard), Typically ≤ 5 days (requery)
Preferred Specimen
BD Vacutainer Whole Blood K2 EDTA Collection Tube 4mL or Oragene Dx Saliva Collection Kit
Shipping Instructions
Specimens to arrive at Helix within 96 hours of collection at ambient temperature.
Clinical Description
This panel evaluates 27 genes associated with hereditary lipidemia.
Ready to order this test?
Contact our clinical team to order the Comprehensive Lipidemia Panel for your patients.