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Searched: Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene/1000

Search Results

Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene

Test Code

Method

Price

7851

Sequencing with CNV PG-Select

$990
Hematology Genetic Tests

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Cholestasis Panel

Test Code

Method

Price

10319

Sequencing with CNV PGxome

$990
Congenital Anomalies of the Gastrointestinal Tract Panel

Test Code

Method

Price

13377

Sequencing with CNV PGxome

$1290
All

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PGmax^TM - Comprehensive Inherited Metabolic Disorders and Mitochondrial Disorders (Nuclear Genes only) Panel

Test Code

Method

Price

16006

Sequencing with CNV PGxome

$1790
Mirum Pharmaceuticals Cholestasis Sponsored Testing

……
Test By Disease

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Dravet Syndrome and Generalized Epilepsy with Febrile Seizures Plus via the SCN1A Gene

Test Code

Method

Price

3043

Sequencing with CNV PG-Select

$990
Lujan Syndrome, FG Syndrome Type 1 and Ohdo Syndrome via the MED12 Gene

Test Code

Method

Price

7991

Sequencing with CNV PG-Select

$990
Timothy Syndrome and Brugada Syndrome via the CACNA1C Gene

Test Code

Method

Price

11123

Sequencing with CNV PGxome

$990

1012

Sanger Sequencing

$2110
Generalized Epilepsy with Febrile Seizures Plus and Dravet syndrome via the SCN1B Gene

Test Code

Method

Price

10671

Sequencing with CNV PG-Select

$990
Meckel-Gruber Syndrome / Joubert Syndrome via the TCTN2 Gene

Test Code

Method

Price

576

Sanger Sequencing

$1010

11041

Sequencing with CNV PGxome

$990
Oculofaciocardiodental Syndrome and Lenz Microphthalmia Syndrome via the BCOR Gene

Test Code

Method

Price

11105

Sequencing with CNV PGxome

$990

949

Sanger Sequencing

$1250
Pierson Syndrome and Congenital Nephrotic Syndrome via the LAMB2 Gene

Test Code

Method

Price

11443

Sequencing with CNV PGxome

$990

556

Sanger Sequencing

$1620
Sick Sinus Syndrome and Brugada Syndrome via the HCN4 Gene

Test Code

Method

Price

11369

Sequencing with CNV PGxome

$990

947

Sanger Sequencing

$960
Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1G Gene

Test Code

Method

Price

11651

Sequencing with CNV PGxome

$990

1274

Sanger Sequencing

$780
News

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Congenital Variant Rett syndrome or FOXG1 syndrome via the FOXG1 Gene

Test Code

Method

Price

8637

Sequencing with CNV PG-Select

$990
Joubert Syndrome, Meckel-Gruber Syndrome, and Nephronophthisis via the TMEM67 Gene

Test Code

Method

Price

15205

Sequencing with CNV PG-Select

$990

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Search Results

Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene

Hematology Genetic Tests

Cholestasis Panel

Congenital Anomalies of the Gastrointestinal Tract Panel

All

PGmax^TM - Comprehensive Inherited Metabolic Disorders and Mitochondrial Disorders (Nuclear Genes only) Panel

Mirum Pharmaceuticals Cholestasis Sponsored Testing

Test By Disease

Dravet Syndrome and Generalized Epilepsy with Febrile Seizures Plus via the SCN1A Gene

Lujan Syndrome, FG Syndrome Type 1 and Ohdo Syndrome via the MED12 Gene

Timothy Syndrome and Brugada Syndrome via the CACNA1C Gene

Generalized Epilepsy with Febrile Seizures Plus and Dravet syndrome via the SCN1B Gene

Meckel-Gruber Syndrome / Joubert Syndrome via the TCTN2 Gene

Oculofaciocardiodental Syndrome and Lenz Microphthalmia Syndrome via the BCOR Gene

Pierson Syndrome and Congenital Nephrotic Syndrome via the LAMB2 Gene

Sick Sinus Syndrome and Brugada Syndrome via the HCN4 Gene

Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1G Gene

News

Congenital Variant Rett syndrome or FOXG1 syndrome via the FOXG1 Gene

Joubert Syndrome, Meckel-Gruber Syndrome, and Nephronophthisis via the TMEM67 Gene