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Primary Ciliary Dyskinesia (PCD) via the RSPH9 Gene

Test Code

Method

Price

748

Sanger Sequencing

$540

9037

Sequencing with CNV PGxome

$890
Primary Ciliary Dyskinesia (PCD) via the RSPH4A Gene

Test Code

Method

Price

747

Sanger Sequencing

$690

8513

Sequencing with CNV PGxome

$890
Bohring-Opitz Syndrome via the ASXL1 Gene

Test Code

Method

Price

2298

Sanger Sequencing

$1280

9827

Sequencing with CNV PGxome

$890
Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome via the MBTPS2 Gene

Test Code

Method

Price

2114

Sanger Sequencing

$810

9823

Sequencing with CNV PGxome

$890
Brugada Syndrome via the SCN3B Gene

Test Code

Method

Price

1017

Sanger Sequencing

$580

8845

Sequencing with CNV PGxome

$890
Congenital Stationary Night Blindness via the LRIT3 Gene

Test Code

Method

Price

2434

Sanger Sequencing

$710

8467

Sequencing with CNV PGxome

$890
Mitochondrial Hypomagnesemia via the SARS2 Gene

Test Code

Method

Price

4977

Sequencing with CNV PGxome

$890
Ichthyosis Bullosa, Siemens via the KRT2 Gene

Test Code

Method

Price

2554

Sanger Sequencing

$780

8381

Sequencing with CNV PGxome

$890
Autosomal Dominant Retinitis Pigmentosa via the PRPF6 Gene

Test Code

Method

Price

4915

Sequencing with CNV PGxome

$890
Hereditary Cancer Testing at PreventionGenetics

…and openly published on our website. Please see our billing page for more information about institutional/provider billing, insurance billing or direct patient billing (self-pay). New panel options We’ve listened and want to meet your testing…
Retinitis Pigmentosa 58 (RP58) via the ZNF513 Gene

Test Code

Method

Price

2452

Sanger Sequencing

$650

8693

Sequencing with CNV PGxome

$890
Premature Ovarian Failure via the STAG3 Gene

Test Code

Method

Price

11877

Sequencing with CNV PGxome

$890
Idiopathic Hypogonadotropic Hypogonadism (IHH) via the TACR3 Gene

Test Code

Method

Price

1747

Sanger Sequencing

$650

8661

Sequencing with CNV PGxome

$890
Galloway-Mowat Syndrome (GAMOS) via the GON7 Gene

Test Code

Method

Price

13091

Sequencing with CNV PGxome

$890
Dilated Cardiomyopathy via the NEXN Gene

Test Code

Method

Price

4197

Sequencing with CNV PGxome

$890
HOXD13-Related Disorders via the HOXD13 Gene

Test Code

Method

Price

10267

Sequencing with CNV PGxome

$890

2332

Sanger Sequencing

$580
Rapid Exome Testing at PreventionGenetics

…that allow patients to receive the answers they need quickly. This includes our Rapid PGxome® test—whole exome sequencing (WES) test—and Neonatal Crisis (NICU) panel. Both tests have an expedited average turnaround time of 14 days…
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…Menu Menu Testing Test Menu PGnome PGxome Custom Panels Tests by Category Targeted Variants How To Order Prenatal All Tests Tests by Disease Partner Programs Sponsored Testing Partnership Information Billing Billing Information Billing…
Thrombocytopenia 4 via the CYCS Gene

Test Code

Method

Price

10047

Sequencing with CNV PGxome

$890

1722

Sanger Sequencing

$370
Leigh Syndrome Associated with Mitochondrial Complex I Deficiency via the NDUFA9 Gene

Test Code

Method

Price

3307

Sanger Sequencing

$910

8207

Sequencing with CNV PGxome

$890

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Custom Panel

Search Results

Primary Ciliary Dyskinesia (PCD) via the RSPH9 Gene

Primary Ciliary Dyskinesia (PCD) via the RSPH4A Gene

Bohring-Opitz Syndrome via the ASXL1 Gene

Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome via the MBTPS2 Gene

Brugada Syndrome via the SCN3B Gene

Congenital Stationary Night Blindness via the LRIT3 Gene

Mitochondrial Hypomagnesemia via the SARS2 Gene

Ichthyosis Bullosa, Siemens via the KRT2 Gene

Autosomal Dominant Retinitis Pigmentosa via the PRPF6 Gene

Hereditary Cancer Testing at PreventionGenetics

Retinitis Pigmentosa 58 (RP58) via the ZNF513 Gene

Premature Ovarian Failure via the STAG3 Gene

Idiopathic Hypogonadotropic Hypogonadism (IHH) via the TACR3 Gene

Galloway-Mowat Syndrome (GAMOS) via the GON7 Gene

Dilated Cardiomyopathy via the NEXN Gene

HOXD13-Related Disorders via the HOXD13 Gene

Rapid Exome Testing at PreventionGenetics

All

Thrombocytopenia 4 via the CYCS Gene

Leigh Syndrome Associated with Mitochondrial Complex I Deficiency via the NDUFA9 Gene