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Hereditary Hemochromatosis Panel

Summary and Pricing

Test Method

Exome Sequencing with CNV Detection
Test Code Test Copy Genes Gene CPT Codes Copy CPT Codes
FTH1 81479,81479
FTL 81479,81479
HAMP 81479,81479
HFE 81479,81479
HJV 81479,81479
SLC40A1 81479,81479
TFR2 81479,81479
Test Code Test Copy Genes Panel CPT Code Gene CPT Codes Copy CPT Code Base Price
10243Genes x (7)81479 81479(x14) $990 Order Options and Pricing

Pricing Comments

We are happy to accommodate requests for testing single genes in this panel or a subset of these genes. The price will remain the list price. If desired, free reflex testing to remaining genes on panel is available. Alternatively, a single gene or subset of genes can also be ordered via our Custom Panel tool.

An additional 25% charge will be applied to STAT orders. STAT orders are prioritized throughout the testing process.

Click here for costs to reflex to whole PGxome (if original test is on PGxome Sequencing platform).

Click here for costs to reflex to whole PGnome (if original test is on PGnome Sequencing platform).

Turnaround Time

3 weeks on average for standard orders or 2 weeks on average for STAT orders.

Please note: Once the testing process begins, an Estimated Report Date (ERD) range will be displayed in the portal. This is the most accurate prediction of when your report will be complete and may differ from the average TAT published on our website. About 85% of our tests will be reported within or before the ERD range. We will notify you of significant delays or holds which will impact the ERD. Learn more about turnaround times here.

Targeted Testing

For ordering sequencing of targeted known variants, go to our Targeted Variants page.


Genetic Counselors


  • Luke Drury, PhD

Clinical Features and Genetics

Clinical Features

Hereditary Hemochromatosis (HH) is a disorder characterized by excess iron overload, which, if untreated, can lead to progressive and potentially fatal organ dysfunction. Chronic iron deposition can result in liver cirrhosis, hepatocellular carcinoma, cardiomyopathy, diabetes, fatigue, and hypogonadism. There are six types of hemochromatosis, each due to a different genetic cause: type 1- HFE, type 2- HAMP or HFE2/HJV, type 3- TFR2, type 4- SLC40A1, type 5- FTH1, and type 6- FTL (Santos et al. 2012). Penetrance of type I HH is variable with many individuals remaining asymptomatic. Disease onset typically occurs after the fourth decade of life with penetrance for type I HH being influenced by other factors including alcohol consumption, fatty liver disease, and co-occurring pathogenic variants in other hemochromatosis related genes (Andersen et al. 2004). Type II HH, also referred to as juvenile HH, is a more severe form of disease with symptom onset occurring with the first or second decade of life. Phlebotomy is the standard treatment for HH and can minimize iron deposition leading to chronic disease. Genetic testing is helpful in the differential diagnosis of HH from other disorders presenting with iron overload including thalassemia, hemolytic anemia, chronic liver disease, and aceruloplasminemia (Bacon et al 2011).


Hemochromatosis is inherited in an autosomal recessive manner through pathogenic variants in the HFE, HAMP, HFE2/HJV, or TFR2 genes or an autosomal dominant manner through pathogenic variants in the SLC40A1, FTH1, or FTL genes (Santos et al. 2012). Type I HH is the most common form. In patients identified with type I HH via transferring saturation analysis, 60% of patients are homozygous for c.845G>A (p.Cys282Tyr), 8% homozygous for c.187C>G (p.His63Asp), and 7% compound heterozygous for these two variants in the HFE gene (de Villiers et al. 1999; Stuhrmann et al. 2010). Co-occurring pathogenic variants in the HAMP and HFE2/HJV genes have been reported in individuals with more severe forms of type I HH (Jacolot et al. 2004; Le Gac et al. 2004). Other forms of HH exhibit higher but variable penetrance for disease compared to type I HH. See individual test descriptions for additional information on the molecular biology of each gene.

Clinical Sensitivity - Sequencing with CNV PGxome

Analytical sensitivity for detection of causative variants in the HFE gene is >95% as gross gene deletions have been reported in very few cases (Le Gac et al. 2008). HJV, HAMP, SLC40A1, TFR2, FTH1, and FTL analytical sensitivity is >99%. In patients where type I HH is clearly defined and other causes of iron overload have been ruled out, clinical sensitivity is >90% in Northern Europeans (Bryant et al. 2008). In a series of 34 patients with juvenile HH, pathogenic variants in HFE2/HJV were found in all cases (Lanzara et al. 2004). However, additional reports suggest that pathogenic variants in the HAMP gene occur in >10% of juvenile HH patients (Goldberg 2011). Clinical sensitivity for the TFR2, FTH1, and FTL genes is currently unknown due to the small number of patients reported to date.

Testing Strategy

This test is performed using Next-Gen sequencing with additional Sanger sequencing as necessary.

This panel provides 100% coverage of all coding exons of the genes plus 10 bases of flanking noncoding DNA in all available transcripts along with other non-coding regions in which pathogenic variants have been identified at PreventionGenetics or reported elsewhere. We define coverage as ≥20X NGS reads or Sanger sequencing. PGnome panels typically provide slightly increased coverage over the PGxome equivalent. PGnome sequencing panels have the added benefit of additional analysis and reporting of deep intronic regions (where applicable).

Dependent on the sequencing backbone selected for this testing, discounted reflex testing to any other similar backbone-based test is available (i.e., PGxome panel to whole PGxome; PGnome panel to whole PGnome).

Indications for Test

The American Association for the Study of Liver Diseases recommends genetic testing of individuals with transferrin saturation levels greater than 45% and with serum ferritin levels greater than 200 ng/ml in males and 150 ng/ml in females (Bacon et al. 2011). Individuals with MRI imaging indicating hepatic iron overload are also candidates for testing (Goldberg 1993).


Official Gene Symbol OMIM ID
FTH1 134770
FTL 134790
HAMP 606464
HFE 613609
HJV 608374
SLC40A1 604653
TFR2 604720
Inheritance Abbreviation
Autosomal Dominant AD
Autosomal Recessive AR
X-Linked XL
Mitochondrial MT

Related Test



  • Andersen R.V. et al. 2004. Blood. 103: 2914-9. PubMed ID: 15070663
  • Bacon B.R. et al. 2011. Hepatology (baltimore, Md.). 54: 328-43. PubMed ID: 21452290
  • Bryant J. et al. 2008. Journal of Medical Genetics. 45: 513-8. PubMed ID: 18310265
  • de Villiers J.N. et al. 1999. Human Molecular Genetics. 8: 1517-22. PubMed ID: 10401000
  • Goldberg Y.P. 2011. Juvenile Hereditary Hemochromatosis. In: Pagon RA, Adam MP, Bird TD, Dolan CR, Fong C-T, Smith RJ, and Stephens K, editors. GeneReviews™, Seattle (WA): University of Washington, Seattle. PubMed ID: 20301349
  • Jacolot S. et al. 2004. Blood. 103: 2835-40. PubMed ID: 14670915
  • Lanzara C. et al. 2004. Blood. 103: 4317-21. PubMed ID: 14982873
  • Le Gac G. et al. 2004. Human Molecular Genetics. 13: 1913-8. PubMed ID: 15254010
  • Le Gac G. et al. 2008. Blood. 112: 5238-40. PubMed ID: 18809761
  • Santos P.C. et al. 2012. International Journal of Molecular Sciences. 13: 1497-511. PubMed ID: 22408404
  • Stuhrmann M. et al. 2010. European Journal of Human Genetics : Ejhg. 18: N/A. PubMed ID: 20125190


Ordering Options

We offer several options when ordering sequencing tests. For more information on these options, see our Ordering Instructions page. To view available options, click on the Order Options button within the test description.

myPrevent - Online Ordering

  • The test can be added to your online orders in the Summary and Pricing section.
  • Once the test has been added log in to myPrevent to fill out an online requisition form.
  • PGnome sequencing panels can be ordered via the myPrevent portal only at this time.

Requisition Form

  • A completed requisition form must accompany all specimens.
  • Billing information along with specimen and shipping instructions are within the requisition form.
  • All testing must be ordered by a qualified healthcare provider.

For Requisition Forms, visit our Forms page

If ordering a Duo or Trio test, the proband and all comparator samples are required to initiate testing. If we do not receive all required samples for the test ordered within 21 days, we will convert the order to the most effective testing strategy with the samples available. Prior authorization and/or billing in place may be impacted by a change in test code.

Specimen Types

Specimen Requirements and Shipping Details

PGxome (Exome) Sequencing Panel

PGnome (Genome) Sequencing Panel

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2) Select Additional Test Options

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Note: acceptable specimen types are whole blood and DNA from whole blood only.
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