Clarity Genetics Super Panel

The Clarity Genetics Super Panel is one of the world's largest, most precise, and thorough tests for detecting genetic markers for 113 of the most common genetic diseases that may affect pregnancy and future child development.

Clarity Genetics Super Panel

What Is It?

The Clarity Genetics Super Panel screens for common genetic conditions across multiple ethnicities, such as cystic fibrosis, sickle cell anemia, and Tay-Sachs. It also screens for conditions that are more rare such as Krabbe and Zellweger syndrome. While many individuals have not heard of the conditions listed on the Super Panel, these genetic conditions can cause a variety of health concerns, including intellectual delay or developmental delays that may necessitate life-long management.

To learn more about the Super Panel, download the brochure. The Clarity Genetics Super Panel can detect your risk for carrying the following genetic diseases:

3-Phosphoglycerate Dehydrogenase deficiency
ABCC8-related Hyperinsulinism
Alpha Thalassemia
Alport syndrome, autosomal recessive
Andermann Syndrome
Arthrogryposis, mental retardation, and seizures (AMRS)
Ataxia With Vitamin E Deficiency
Autosomal Recessive Polycystic Kidney Disease
Bardet-Biedl Syndrome, BBS1-related
Bardet-Biedl Syndrome, BBS10-related
Beta Thalassemia
Biotinidase Deficiency
Bloom Syndrome
Canavan Disease
Carnitine Palmitoyltransferase IA Deficiency
Carnitine Palmitoyltransferase II Deficiency
Cartilage-Hair Hypoplasia
Classic Citrullinemia
CLN3-related Neuronal Ceroid Lipofuscinosis
CLN5-related Neuronal Ceroid Lipofuscinosis
Cohen Syndrome
Congenital Amegakaryocytic Thrombocytopenia
Congenital Disorder of Glycosylation Type Ia
Congenital Disorder of Glycosylation Type Ib
Congenital Finnish Nephrosis
Costeff Optic Atrophy Syndrome
Cystic Fibrosis
D-Bifunctional Protein Deficiency
Dihydrolipoamide Dehydrogenase Deficiency
Dyskeratosis Congenita, autosomal recessive
Ehlers-Danlos, type VIIC
Factor XI Deficiency
Familial Dysautonomia
Familial Mediterranean Fever
Fanconi Anemia Type C
Fragile X
Gaucher Disease
GJB2-related DFNB1 Nonsyndromic Hearing Loss and Deafness
Glucose-6-Phosphate Dehydrogenase Deficiency
Glutaric Acidemia Type 1
Glycogen Storage Disease Type Ia
Glycogen Storage Disease Type Ib
Glycogen Storage Disease Type III
Glycogen Storage Disease Type V
GRACILE Syndrome
Hereditary Fructose Intolerance
Hereditary Thymine-Uraciluria
Hurler Syndrome
Hypophosphatasia, Autosomal Recessive
Inclusion Body Myopathy 2
Isovaleric Acidemia
Joubert Syndrome 2
Krabbe Disease
LAMA3-related Junctional Epidermolysis Bullosa
LAMB3-related Junctional Epidermolysis Bullosa
LAMC2-related Junctional Epidermolysis Bullosa
Limb-Girdle Muscular Dystrophy Type 2D
Limb-Girdle Muscular Dystrophy Type 2E
Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
Maple Syrup Urine Disease Type I
Medium Chain Acyl-CoA Dehydrogenase Deficiency
Megalencephalic Leukoencephalopathy With Subcortical Cysts
Metachromatic Leukodystrophy
Mucolipidosis IV
Multiple Sulphatase deficiency
Muscle-Eye-Brain Disease
NEB-related Nemaline Myopathy
Niemann-Pick Disease Type C
Niemann-Pick Disease, SMPD1-associated
Nijmegen Breakage Syndrome
Northern Epilepsy
Pendred Syndrome
PEX1-related Zellweger Syndrome Spectrum
Phenylalanine Hydroxylase Deficiency
Polyglandular Autoimmune Syndrome Type 1
Pompe Disease
PPT1-related Neuronal Ceroid Lipofuscinosis
Primary Carnitine Deficiency
Primary Hyperoxaluria Type 1
Primary Hyperoxaluria Type 2
PROP1-related Combined Pituitary Hormone Deficiency
Retinitis Pigmentosa 59
Rhizomelic Chondrodysplasia Punctata Type 1
Salla Disease
Segawa Syndrome
Short Chain Acyl-CoA Dehydrogenase Deficiency**
Sickle Cell Anemia
Sjogren-Larsson Syndrome
Smith-Lemli-Opitz Syndrome
Spinal Muscular Atrophy
Steroid-Resistant Nephrotic Syndrome
Sulfate Transporter-Related Osteochondrodysplasia
Tay-Sachs Disease
TPP1-related Neuronal Ceroid Lipofuscinosis
Tyrosinemia Type I
Usher Syndrome Type 1F
Usher Syndrome Type 3
Very Long Chain Acyl-CoA Dehydrogenase Deficiency
Wilson Disease
X-Linked Juvenile Retinoschisis

Who Should Take It?

• All individuals of child bearing age, regardless of gender
• All individuals with a family history of genetic disorders
• All individuals with partners who are carriers of genetic disorders
• Those considering in vitro fertilization
• Pregnant women

Why Clarity Genetics?

When testing, our laboratory analyzes all of the coding DNA in a gene to determine if any disease-causing pathogenic variants are present. By sequencing all of the coding DNA in a gene, instead of just a portion, we are able to offer the most accurate genetic testing available, regardless of your ethnicity. The majority of laboratories are only sequencing a portion of the gene, leaving room for error with missed pathogenic variants, especially when testing a variety of ethnicities. By sequencing the entire gene, Clarity Genetics testing eliminates the doubt in a negative result and drastically reduces the residual risk, regardless of ethnicity.

Talk to a Genetic Counselor

As a Clarity client, you'll have access to personal genetic counselors who can help explain the results of your screens and provide insight on how to move forward. To schedule a personal conference to discuss your screen results, click the link below or call(866) 661-7966​

Discuss Your Screening Results

Connect With Our Customer Care Center

Get answers to all your questions related to billing, insurance coverage, the status of your screening results, and more by calling us at (866) 661-7966​ or clicking the link below.

Connect With Our  Customer Care Center