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Genetics at Oasis

You are unique and so is your genetic make up.  Genetic screening can help guide us to live better and healthier lives. At Oasis MD, we have partnered with knowledgeable experts and accredited laboratories to bring the most accurate, trusted, and advanced testing within convenient reach.

Paint a more complete and personalized picture of your health and disease prevention with the power of genetic screening today.

Tests Offered

Non-invasive Prenatal Screening (NIPS/NIPT)

Coming Soon

Analyzes whether a pregnancy is at increased risk for chromosomal disorders. NIPS is recommended as a first tier screening test for common trisomies (21, 18, and 13) by the Society of Obstetricians and Gynecologists of Canada. This test must be done after 10 weeks of gestations. Whether testing is appropriate for your pregnancy should be discussed with your health care provider.

Conditions that can be tested include:

  • Trisomy 13 (Patau syndrome)
  • Trisomy 18 (Edwards syndrome)
  • Trisomy 21 (Down syndrome)
  • Sex chromosome aneuploidies
  • Additional rare autosomal trisomies and microdeletion testing available as well

Complete Genetic Health Screening

This test is intended for use to screen individuals for hereditary conditions that, if detected early, may have effective medical interventions and preventive measures.

Conditions tested include:

  • Cancers
  • Cardiovascular diseases
  • Metabolic diseases
  • Other medically actionable conditions
  • 167 genes tested

Cancer Genetic Screen

This test is meant for screening individuals for genetically susceptible conditions to hereditary cancers. If detected early there may be effective medical interventions or preventative measures.

Conditions tested include but not limited to:

  • Breast cancer
  • Colorectal cancer
  • Cutaneous melanoma
  • Gastric cancer
  • Ovarian cancer
  • Pancreatic cancer
  • Prostate cancer
  • Renal cell cancer
  • Thyroid cancer
  • Uterine cancer
  • 65 genes tested

Cardiovascular Genetic Screen

This test is meant for screening individuals for hereditary cardiovascular conditions. If detected early there may be effective medical interventions or preventative measures.

Conditions tested include but not limited to:

  • Aortopathies
  • Arrhythmias
  • Cardiomyopathies
  • Genetic forms of high cholesterol
  • Thrombophilia

Pharmacogenomics Testing

Analyzes a broad panel of genes that could impact clinical response to medications and is intended to aid clinicians with medication and dosage selection. Pharmacogenomic results should be used in combination with other clinical considerations and therapeutic drug monitoring to optimize treatment regimens and ensure safe medication use.

  • 38 genes tested

*Prices show above may change without notice. Please inquire for up to date pricing.

All genetic screening tests are not comprehensive and does not include the entirety of all cancers or diseases stated above. Many cancers and heart conditions may genetic predispositions that does not have a genetic tests available.

All test specimens are shipped to a College of American Pathologists (CAP)-accredited and Clinical Laboratory Improvement Amendments (CLIA)-certified clinical diagnostic laboratory performing full-gene sequencing and deletion/duplication analysis using next-generation sequencing technology (NGS).

Get in touch to start your personalized health journey.

Call us today at 604 630 3833
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  • ATM-related conditions
  • BARD1-related conditions
  • EGFR-related conditions
  • KIT-related conditions
  • LMNA-related conditions
  • MITF-related conditions
  • NTHL1-associated polyposis
  • POLD1-related conditions
  • POLE-related conditions
  • POT1-related conditions
  • PRKAR1A-related conditions
  • PTEN-related conditions
  • SMARCA4-related tumors
  • Acute intermittent porphyria (AIP)
  • Alpha-1 antitrypsin deficiency (AATD)
  • Andersen-Tawil syndrome
  • Antithrombin III deficiency
  • Arrhythmogenic cardiomyopathy
  • Arrhythmogenic right ventricular cardiomyopathy (ARVC)
  • Atrial fibrillation
  • Autosomal dominant oligodontia-colorectal cancer syndrome
  • BAP1-related conditions
  • Basal cell nevus syndrome (BCNS) / Gorlin Syndrome
  • Biotinidase deficiency
  • Birt-Hogg-Dubé (BHD) syndrome
  • BRCA1/BRCA2-Associated Hereditary breast and ovarian cancer (HBOC) syndrome
  • BRIP1-related cancer risk
  • Brugada syndrome (BrS)
  • Carvajal syndrome
  • Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)
  • CDC73-related conditions
  • CDK4-related cutaneous melanoma
  • CHEK2-related conditions
  • Coffin-Siris syndrome
  • Constitutional mismatch repair deficiency syndrome (CMMR-D)
  • Danon disease
  • DICER1-related pleuropulmonary blastoma familial tumor predisposition syndrome
  • Dilated cardiomyopathy (DCM)
  • Dystonia
  • Dystrophinopathy
  • Ehlers-Danlos syndrome (EDS), classic type (types I/II)
  • Ehlers-Danlos syndrome (EDS), vascular type (type IV)
  • Emery-Dreifuss muscular dystrophy
  • Fabry disease
  • Factor IX deficiency
  • Factor V Leiden-related thrombophilia
  • Familial adenomatous polyposis (FAP), Attenuated familial adenomatous polyposis (AFAP)
  • Familial erythrocytosis
  • Familial hypercholesterolemia (FH)
  • Familial Mediterranean fever
  • Fanconi Anemia
  • FH-related conditions
  • GIST-plus syndrome
  • Glycogen storage disease type II (GSDII), also known as Pompe disease
  • Hereditary diffuse gastric cancer (HDGC)
  • Hereditary hemochromatosis
  • Hereditary hemorrhagic telangiectasia (HHT)
  • Hereditary mixed polyposis syndrome
  • Hereditary paraganglioma-pheochromocytoma (PGL-PCC) syndrome
  • Hereditary transthyretin-mediated amyloidosis (hATTR amyloidosis)
  • Hirschsprung disease
  • HOXB13-related predisposition to prostate cancer
  • Hypertrophic cardiomyopathy (HCM)
  • Inherited cardiomyopathies
  • Inherited retinal dystrophy (IRD)
  • Jervell and Lange-Nielsen syndrome (JLNS)
  • Juvenile polyposis syndrome (JPS)
  • Left ventricular noncompaction (LVNC)
  • Li Fraumeni syndrome (LFS)
  • Limb-girdle muscular dystrophy type 2F
  • Loeys-Dietz syndrome (LDS)
  • Long QT syndrome
  • Lynch syndrome
  • Malignant hyperthermia susceptibility (MHS)
  • Marfan syndrome and other FBN1-related conditions
  • Melanoma-pancreatic cancer syndrome and melanoma-neural system tumor syndrome
  • MET-related conditions
  • MODY
  • MSH3-associated polyposis
  • Multiple endocrine neoplasia type 1 (MEN1)
  • Multiple endocrine neoplasia type 2 (MEN2)
  • Multiple endocrine neoplasia type 4 (MEN4)
  • MUTYH-associated polyposis (MAP)
  • Myhre syndrome
  • Myofibrillar Myopathy
  • Naxos disease
  • Neurofibromatosis type 1 (NF1)
  • Neurofibromatosis type 2
  • NKX2-5-related conditions
  • Noonan spectrum disorders (NSDs) / RASopathies
  • Ornithine transcarbamylase (OTC) deficiency
  • PALB2-related conditions
  • Peutz-Jeghers syndrome (PJS)
  • Protein C deficiency
  • Protein S deficiency
  • Prothrombin-related thrombophilia
  • Pulmonary arterial hypertension (PAH)
  • RAD51C-related cancers
  • RAD51D-related cancers
  • Red blood cell enzymopathies
  • Renal cysts and diabetes syndrome
  • Restrictive cardiomyopathy (RCM)
  • Retinoblastoma (Rb)
  • RYR1-related conditions
  • Schwannomatosis
  • Short QT syndrome
  • SMARCB1-related tumors
  • Smooth muscle dysfunction syndrome
  • Thoracic aortic aneurysms and aortic dissections (TAAD)
  • Timothy syndrome
  • Tuberous sclerosis complex
  • von Hippel-Lindau syndrome
  • Wilson disease
  • Wolff-Parkinson-White syndrome (WPW)
  • WT1-related disorders
  • X-linked adrenoleukodystrophy (X-ALD)
  • ATM-related conditions
  • BARD1-related conditions
  • EGFR-related conditions
  • KIT-related conditions
  • MITF-related conditions
  • NTHL1-associated polyposis
  • POLD1-related conditions
  • POLE-related conditions
  • POT1-related conditions
  • PRKAR1A-related conditions
  • PTEN-related conditions
  • SMARCA4-related tumors
  • Autosomal dominant oligodontia-colorectal cancer syndrome
  • BAP1-related conditions
  • Basal cell nevus syndrome (BCNS) / Gorlin Syndrome
  • Birt-Hogg-Dubé (BHD) syndrome
  • BRCA1/BRCA2-Associated Hereditary breast and ovarian cancer (HBOC) syndrome
  • BRIP1-related cancer risk
  • CDC73-related conditions
  • CDK4-related cutaneous melanoma
  • CHEK2-related conditions
  • Coffin-Siris syndrome
  • Constitutional mismatch repair deficiency syndrome (CMMR-D)
  • DICER1-related pleuropulmonary blastoma familial tumor predisposition syndrome
  • Familial adenomatous polyposis (FAP), Attenuated familial adenomatous polyposis (AFAP)
  • Familial erythrocytosis
  • Familial isolated pituitary adenoma (FIPA)
  • Fanconi Anemia
  • FH-related conditions
  • GIST-plus syndrome
  • Hereditary diffuse gastric cancer (HDGC)
  • Hereditary mixed polyposis syndrome
  • Hereditary paraganglioma-pheochromocytoma (PGL-PCC) syndrome
  • Hirschsprung disease
  • HOXB13-related predisposition to prostate cancer
  • Juvenile polyposis syndrome (JPS)
  • Li Fraumeni syndrome (LFS)
  • Lynch syndrome
  • Melanoma-pancreatic cancer syndrome and melanoma-neural system tumor syndrome
  • MET-related conditions
  • MSH3-associated polyposis
  • Multiple endocrine neoplasia type 1 (MEN1)
  • Multiple endocrine neoplasia type 2 (MEN2)
  • Multiple endocrine neoplasia type 4 (MEN4)
  • MUTYH-associated polyposis (MAP)
  • Neurofibromatosis type 1 (NF1)
  • Noonan spectrum disorders (NSDs) / RASopathies
  • PALB2-related conditions
  • Peutz-Jeghers syndrome (PJS)
  • RAD51C-related cancers
  • RAD51D-related cancers
  • Retinoblastoma (Rb)
  • Schwannomatosis
  • SMARCB1-related tumors
  • Tuberous sclerosis complex
  • von Hippel-Lindau syndrome
  • WT1-related disorders
  • Andersen-Tawil syndrome
  • Antithrombin III deficiency
  • Arrhythmogenic cardiomyopathy
  • Arrhythmogenic right ventricular cardiomyopathy (ARVC)
  • Atrial fibrillation
  • Brugada syndrome (BrS)
  • Carvajal syndrome
  • Catecholaminergic Polymorphic Ventricular Tachycardia
  • Danon disease
  • Dilated cardiomyopathy (DCM)
  • Dystrophinopathy
  • Ehlers-Danlos syndrome (EDS), classic type (types I/II)
  • Ehlers-Danlos syndrome (EDS), vascular type (type IV)
  • Emery-Dreifuss muscular dystrophy
  • Fabry disease
  • Factor IX deficiency (hemophilia B)
  • Factor V Leiden-related thrombophilia
  • Familial hypercholesterolemia (FH)
  • Hereditary hemorrhagic telangiectasia (HHT)
  • Hereditary transthyretin-mediated amyloidosis (hATTR amyloidosis)
  • Hypertrophic cardiomyopathy (HCM)
  • Jervell and Lange-Nielsen syndrome (JLNS)
  • Left ventricular noncompaction (LVNC)
  • Limb-girdle muscular dystrophy type 2F
  • Loeys-Dietz syndrome (LDS)
  • Long QT syndrome
  • Marfan syndrome and other FBN1-related conditions
  • Myofibrillar Myopathy
  • Naxos disease
  • NKX2-5-related conditions
  • Protein C deficiency
  • Protein S deficiency
  • Prothrombin-related thrombophilia
  • Pulmonary arterial hypertension (PAH)
  • Restrictive cardiomyopathy (RCM)
  • Short QT syndrome
  • Thoracic aortic aneurysms and aortic dissections (TAAD)
  • Timothy syndrome
  • Wolff-Parkinson-White syndrome (WPW)

More information is coming soon