Whole Exome Sequencing Recommendation Form - Cigna: Fill out & sign online

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Click ‘Get Form’ to open the Whole Exome Sequencing Recommendation Form in the editor.
Begin by filling out the Customer (patient) information section. Enter the patient's name, Cigna customer ID, date of birth, and date of consultation.
Next, provide the Ordering health care professional’s information. Include their name, address, specialty, Taxpayer Identification Number (TIN), telephone, and fax number.
If applicable, fill in the Clinical geneticist or genetic counselor's details. Ensure all contact information is accurate.
Complete the Rendering laboratory information section with the lab's name, address, TIN, telephone, and fax.
List any relevant diagnosis codes in the designated area and specify requested test information including test name and CPT code(s).
Indicate if the patient’s phenotype is likely genetic by checking appropriate boxes and providing necessary details.
Fill out sections for differential diagnoses and key gene(s) of interest as needed.
Review your entries for accuracy before signing at the bottom of the form. Make sure to attach required documents as specified.

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Is whole exome sequencing worth it?

Genome Sequencing Cost In 2025 Whole-genome sequencing (WGS) is now projected to cost approximately $200 per genome. This is made possible by leading companies like Illumina and emerging competitors such as Ultima Genomics, which are making a huge leap into this field.

What is the coverage of whole exome sequencing?

Whole exome sequencing (WES) provides coverage of more than 95% of the exons, (the expressed or the protein-coding regions of the genome), which harbor the majority of the large genetic variants and single nucleotide polymorphisms (SNPs) associated with human disease phenotypes.

Does insurance cover whole exome sequencing?

Insurance carriers are increasingly covering exome and genome testing. But as with all medical tests, patients may still receive a bill if they have not yet met their yearly plan deductible or if their plan requires coinsurance. GeneDx offers a variety of Patient Access Solutions to help.

When to order whole exome sequencing?

Whole exome and genome sequencing can also be informative for individuals with a high suspicion for an underlying genetic cause of their clinical features, but where previous genetic tests such as chromosomal microarray, biochemical testing, single gene testing, or multi-gene panels have failed to identify a diagnosis.