Ambry Genetics

Personnel

Director: Elizabeth Chao, MD, Lab Director
Email: [email protected]
Director: Brigette Davis, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
Email: [email protected]
Director: Chia-Ling Gau, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
Email: [email protected]
Julia Thai, BS, Administrator
Email: [email protected]
Elyse Ryan, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
Email: [email protected]
Monalyn Salvador, MS, CGC, Manager, Product Management - Oncology
Phone: 949-457-8961
Email: [email protected]

Conditions and tests

477 conditions/phenotypes with 105 tests
Enter text to narrow down the list

3-Methylglutaconic aciduria type 24 tests
Acromicric dysplasia3 tests
Acute lymphoid leukemia5 tests
Acute myeloid leukemia3 tests
Adams-Oliver syndrome 53 tests
Adrenocortical carcinoma, hereditary6 tests
Alagille syndrome due to a JAG1 point mutation2 tests
Amyloidosis, hereditary systemic 17 tests
Andersen Tawil syndrome3 tests
Aneurysm-osteoarthritis syndrome3 tests
Aortic aneurysm, familial thoracic 43 tests
Aortic aneurysm, familial thoracic 63 tests
Aortic aneurysm, familial thoracic 73 tests
Aortic aneurysm, familial thoracic 83 tests
Aortic valve disorder3 tests
Aplastic anemia5 tests
Arrhythmogenic cardiomyopathy with wooly hair and keratoderma5 tests
Arrhythmogenic right ventricular dysplasia 15 tests
Arrhythmogenic right ventricular dysplasia 105 tests
Arrhythmogenic right ventricular dysplasia 115 tests
Arrhythmogenic right ventricular dysplasia 125 tests
Arrhythmogenic right ventricular dysplasia 26 tests
Arrhythmogenic right ventricular dysplasia 55 tests
Arrhythmogenic right ventricular dysplasia 85 tests
Arrhythmogenic right ventricular dysplasia 95 tests
Arterial tortuosity syndrome3 tests
Ataxia-telangiectasia syndrome11 tests
Ataxia-telangiectasia-like disorder7 tests
ATP1A3-associated neurological disorder1 test
Atrial fibrillation, familial, 106 tests
Atrial fibrillation, familial, 124 tests
Atrial fibrillation, familial, 133 tests
Atrial fibrillation, familial, 142 tests
Atrial fibrillation, familial, 34 tests
Atrial fibrillation, familial, 44 tests
Atrial fibrillation, familial, 93 tests
Atrial septal defect 22 tests
Atrial septal defect 36 tests
Atrial septal defect 44 tests
Atrial septal defect 56 tests
Atrial septal defect 75 tests
Atrioventricular septal defect 42 tests
Autoimmune lymphoproliferative syndrome type 41 test
Autosomal dominant nonsyndromic hearing loss 104 tests
Autosomal recessive limb-girdle muscular dystrophy type 2G8 tests
Autosomal recessive limb-girdle muscular dystrophy type 2J4 tests
Autosomal recessive limb-girdle muscular dystrophy type 2M4 tests
Bannayan-Riley-Ruvalcaba syndrome14 tests
BAP1-related tumor predisposition syndrome5 tests
Basal cell carcinoma, susceptibility to, 13 tests
Basal cell carcinoma, susceptibility to, 76 tests
Becker muscular dystrophy5 tests
Birt-Hogg-Dube syndrome4 tests
Blepharocheilodontic syndrome5 tests
Blepharophimosis - intellectual disability syndrome, MKB type3 tests
Breast and/or ovarian cancer2 tests
Breast cancer, susceptibility to2 tests
Breast-ovarian cancer, familial, susceptibility to1 test
Breast-ovarian cancer, familial, susceptibility to, 114 tests
Breast-ovarian cancer, familial, susceptibility to, 215 tests
Breast-ovarian cancer, familial, susceptibility to, 310 tests
Breast-ovarian cancer, familial, susceptibility to, 49 tests
Bronchiectasis with or without elevated sweat chloride 14 tests
Brugada syndrome 16 tests
Brugada syndrome 23 tests
Brugada syndrome 33 tests
Brugada syndrome 43 tests
Brugada syndrome 53 tests
Brugada syndrome 63 tests
Brugada syndrome 73 tests
Brugada syndrome 83 tests
Brugada syndrome 93 tests
Capillary malformation-arteriovenous malformation syndrome1 test
Carcinoid tumor of intestine4 tests
Carcinoma of colon16 tests
Carcinoma of pancreas18 tests
Cardiac arrhythmia1 test
Cardiac arrhythmia, ankyrin-B-related4 tests
Cardiac valvular dysplasia, X-linked3 tests
Cardiofaciocutaneous syndrome 21 test
Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis5 tests
Cardiomyopathy, familial restrictive, 16 tests
Cardiomyopathy, familial restrictive, 36 tests
Carney-Stratakis syndrome4 tests
Carpal tunnel syndrome7 tests
Cataract 16 multiple types3 tests
Catecholaminergic polymorphic ventricular tachycardia 16 tests
Catecholaminergic polymorphic ventricular tachycardia 24 tests
Catecholaminergic polymorphic ventricular tachycardia 45 tests
Catecholaminergic polymorphic ventricular tachycardia 55 tests
Cerebral arteriovenous malformation1 test
Charcot-Marie-Tooth disease type 2B16 tests
Choroid plexus papilloma6 tests
Chuvash polycythemia1 test
Colorectal cancer, hereditary nonpolyposis, type 214 tests
Colorectal cancer, hereditary nonpolyposis, type 63 tests
Colorectal cancer, susceptibility to, 13 tests
Colorectal cancer, susceptibility to, 1012 tests
Congenital bilateral aplasia of vas deferens from CFTR mutation4 tests
Congenital central hypoventilation3 tests
Congenital contractural arachnodactyly3 tests
Congenital diarrhea 5 with tufting enteropathy6 tests
Congenital muscular dystrophy due to LMNA mutation6 tests
Conotruncal heart malformations5 tests
Cowden syndrome4 tests
Cowden syndrome 115 tests
Cowden syndrome 33 tests
Cystic fibrosis4 tests
Danon disease6 tests
Desmin-related myofibrillar myopathy4 tests
Desmoid disease, hereditary6 tests
Developmental and epileptic encephalopathy, 523 tests
Developmental delay2 tests
Diabetes mellitus type 11 test
Diamond-Blackfan anemia 11 test
Diamond-Blackfan anemia 101 test
Diamond-Blackfan anemia 111 test
Diamond-Blackfan anemia 31 test
Diamond-Blackfan anemia 41 test
Diamond-Blackfan anemia 51 test
Diamond-Blackfan anemia 61 test
Diamond-Blackfan anemia 71 test
Diamond-Blackfan anemia 81 test
Diamond-Blackfan anemia 91 test
DICER1-related tumor predisposition9 tests
DiGeorge syndrome2 tests
Dilated cardiomyopathy 1A6 tests
Dilated cardiomyopathy 1AA6 tests
Dilated cardiomyopathy 1BB5 tests
Dilated cardiomyopathy 1C4 tests
Dilated cardiomyopathy 1CC6 tests
Dilated cardiomyopathy 1D6 tests
Dilated cardiomyopathy 1DD4 tests
Dilated cardiomyopathy 1E7 tests
Dilated cardiomyopathy 1EE6 tests
Dilated cardiomyopathy 1FF6 tests
Dilated cardiomyopathy 1G4 tests
Dilated cardiomyopathy 1HH4 tests
Dilated cardiomyopathy 1I6 tests
Dilated cardiomyopathy 1II3 tests
Dilated cardiomyopathy 1J4 tests
Dilated cardiomyopathy 1JJ4 tests
Dilated cardiomyopathy 1KK6 tests
Dilated cardiomyopathy 1M6 tests
Dilated cardiomyopathy 1NN7 tests
Dilated cardiomyopathy 1O4 tests
Dilated cardiomyopathy 1P6 tests
Dilated cardiomyopathy 1R6 tests
Dilated cardiomyopathy 1S6 tests
Dilated cardiomyopathy 1W6 tests
Dilated cardiomyopathy 1X4 tests
Dilated cardiomyopathy 1Y6 tests
Dilated cardiomyopathy 1Z6 tests
Dilated cardiomyopathy 2A6 tests
Dilated cardiomyopathy 2B3 tests
Dilated cardiomyopathy 3B5 tests
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome6 tests
Distal myopathy, Tateyama type4 tests
Duchenne muscular dystrophy5 tests
Dyskeratosis congenita, autosomal dominant 12 tests
Dyskeratosis congenita, autosomal dominant 22 tests
Dyskeratosis congenita, autosomal dominant 31 test
Dyskeratosis congenita, autosomal recessive 11 test
Dyskeratosis congenita, autosomal recessive 21 test
Dyskeratosis congenita, autosomal recessive 31 test
Dyskeratosis congenita, X-linked1 test
Early-onset myopathy with fatal cardiomyopathy4 tests
Ehlers-Danlos syndrome, classic type, 13 tests
Ehlers-Danlos syndrome, kyphoscoliotic type 13 tests
Ehlers-Danlos syndrome, type 43 tests
Elevated circulating creatine kinase concentration4 tests
Emery-Dreifuss muscular dystrophy 2, autosomal dominant6 tests
Emery-Dreifuss muscular dystrophy 3, autosomal recessive6 tests
Emery-Dreifuss muscular dystrophy 7, autosomal dominant5 tests
Endemic goiter9 tests
Endometrial carcinoma15 tests
Epilepsy, idiopathic generalized, susceptibility to, 121 test
Episodic ataxia type 61 test
Episodic pain syndrome, familial, 21 test
Fabry disease5 tests
Familial adenomatous polyposis 112 tests
Familial adenomatous polyposis 212 tests
Familial adenomatous polyposis 32 tests
Familial cancer of breast22 tests
Familial chylomicronemia syndrome1 test
Familial colorectal cancer2 tests
Familial hyperaldosteronism type III2 tests
Familial hypercholesterolemia1 test
Familial hypobetalipoproteinemia 11 test
Familial medullary thyroid carcinoma5 tests
Familial meningioma6 tests
Familial partial lipodystrophy, Dunnigan type6 tests
Familial spontaneous pneumothorax1 test
Fanconi anemia complementation group D17 tests
Fanconi anemia complementation group J4 tests
Fanconi anemia complementation group N5 tests
Fanconi anemia complementation group O4 tests
Fanconi anemia, complementation group S6 tests
Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young1 test
Fatal infantile hypertonic myofibrillar myopathy3 tests
FG syndrome 13 tests
FG syndrome 23 tests
Fibromatosis, gingival, 11 test
Fragile X syndrome1 test
Friedreich ataxia 15 tests
Frontometaphyseal dysplasia3 tests
Fumarase deficiency1 test
Gastrointestinal stromal tumor4 tests
Geleophysic dysplasia 23 tests
Generalized epilepsy with febrile seizures plus, type 13 tests
Glioma susceptibility 19 tests
Glioma susceptibility 29 tests
Glioma susceptibility 311 tests
Glucocorticoid deficiency 54 tests
Gorlin syndrome1 test
Heart-hand syndrome, Slovenian type6 tests
Hepatic adenomas, familial1 test
Hepatocellular carcinoma12 tests
Hereditary breast ovarian cancer syndrome2 tests
Hereditary cancer1 test
Hereditary cancer-predisposing syndrome5 tests
Hereditary diffuse gastric adenocarcinoma16 tests
Hereditary disease17 tests
Hereditary hemorrhagic telangiectasia1 test
Hereditary leiomyomatosis and renal cell cancer5 tests
Hereditary nonpolyposis colon cancer1 test
Hereditary pancreatitis4 tests
Heterotopia, periventricular, X-linked dominant3 tests
Hirschsprung disease, susceptibility to, 15 tests
Holoprosencephaly 71 test
Holt-Oram syndrome3 tests
Hutchinson-Gilford syndrome6 tests
Hypercholesterolemia, autosomal dominant, 31 test
Hypercholesterolemia, autosomal dominant, type B1 test
Hypercholesterolemia, familial, 41 test
HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED3 tests
Hyperinsulinism due to glucokinase deficiency1 test
Hyperthyroxinemia, dystransthyretinemic7 tests
Hypertrichotic osteochondrodysplasia Cantu type4 tests
Hypertrophic cardiomyopathy 18 tests
Hypertrophic cardiomyopathy 105 tests
Hypertrophic cardiomyopathy 116 tests
Hypertrophic cardiomyopathy 126 tests
Hypertrophic cardiomyopathy 136 tests
Hypertrophic cardiomyopathy 146 tests
Hypertrophic cardiomyopathy 156 tests
Hypertrophic cardiomyopathy 165 tests
Hypertrophic cardiomyopathy 175 tests
Hypertrophic cardiomyopathy 188 tests
Hypertrophic cardiomyopathy 26 tests
Hypertrophic cardiomyopathy 206 tests
Hypertrophic cardiomyopathy 258 tests
Hypertrophic cardiomyopathy 36 tests
Hypertrophic cardiomyopathy 46 tests
Hypertrophic cardiomyopathy 65 tests
Hypertrophic cardiomyopathy 76 tests
Hypertrophic cardiomyopathy 85 tests
Hypertrophic cardiomyopathy 94 tests
Hypoplastic left heart syndrome 25 tests
Hypothyroidism, congenital, nongoitrous, 55 tests
Intellectual disability2 tests
Intellectual disability, autosomal dominant 164 tests
Interstitial lung disease due to ABCA3 deficiency1 test
Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked3 tests
Isolated ectopia lentis3 tests
Jervell and Lange-Nielsen syndrome 14 tests
Jervell and Lange-Nielsen syndrome 24 tests
Joubert syndrome 101 test
Juvenile myelomonocytic leukemia6 tests
Juvenile polyposis syndrome16 tests
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome17 tests
Kartagener syndrome1 test
Keratosis palmoplantaris striata 25 tests
Left ventricular noncompaction 106 tests
Legius syndrome1 test
Leigh syndrome4 tests
LEOPARD syndrome 16 tests
LEOPARD syndrome 27 tests
Lethal acantholytic epidermolysis bullosa5 tests
Lethal congenital glycogen storage disease of heart5 tests
Lethal tight skin contracture syndrome6 tests
Li-Fraumeni syndrome 115 tests
Li-Fraumeni syndrome 215 tests
Linear nevus sebaceous syndrome1 test
Loeys-Dietz syndrome 13 tests
Loeys-Dietz syndrome 23 tests
Long QT syndrome 14 tests
Long QT syndrome 104 tests
Long QT syndrome 114 tests
Long QT syndrome 124 tests
Long QT syndrome 133 tests
Long QT syndrome 145 tests
Long QT syndrome 151 test
Long QT syndrome 161 test
Long QT syndrome 24 tests
Long QT syndrome 36 tests
Long QT syndrome 54 tests
Long QT syndrome 64 tests
Long QT syndrome 94 tests
Lung carcinoma1 test
Lynch syndrome1 test
Lynch syndrome 115 tests
Lynch syndrome 414 tests
Lynch syndrome 514 tests
Lynch syndrome 814 tests
Macrocephaly-autism syndrome6 tests
Macular degeneration, early-onset3 tests
Macular degeneration, X-linked atrophic1 test
Malignant tumor of esophagus3 tests
Malignant tumor of prostate16 tests
Malignant tumor of testis5 tests
Malignant tumor of urinary bladder6 tests
Mandibular hypoplasia-deafness-progeroid syndrome4 tests
Mandibuloacral dysplasia6 tests
Marfan syndrome3 tests
MASS syndrome3 tests
Maturity-onset diabetes of the young type 11 test
Maturity-onset diabetes of the young type 21 test
Maturity-onset diabetes of the young type 31 test
Maturity-onset diabetes of the young type 41 test
Medulloblastoma11 tests
Melanoma and neural system tumor syndrome8 tests
Melanoma, cutaneous malignant, susceptibility to, 19 tests
Melanoma, cutaneous malignant, susceptibility to, 29 tests
Melanoma, cutaneous malignant, susceptibility to, 310 tests
Melanoma, cutaneous malignant, susceptibility to, 84 tests
Melanoma, cutaneous malignant, susceptibility to, 92 tests
Melanoma-pancreatic cancer syndrome8 tests
Melnick-Needles syndrome3 tests
Metachondromatosis6 tests
Microcephaly, normal intelligence and immunodeficiency4 tests
Migraine, familial hemiplegic, 11 test
Migraine, familial hemiplegic, 21 test
Migraine, familial hemiplegic, 31 test
Mismatch repair cancer syndrome 110 tests
Moyamoya disease 53 tests
Muir-Torré syndrome15 tests
Multiple congenital anomalies4 tests
Multiple endocrine neoplasia type 2A5 tests
Multiple endocrine neoplasia type 2B5 tests
Multiple endocrine neoplasia type 44 tests
Multiple endocrine neoplasia, type 15 tests
Multiple self-healing squamous epithelioma3 tests
Multisystemic smooth muscle dysfunction syndrome3 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 44 tests
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B44 tests
MYH7-related skeletal myopathy6 tests
Myhre syndrome15 tests
Myofibrillar myopathy 23 tests
Myofibrillar myopathy 44 tests
Myofibrillar myopathy 64 tests
Myopathy, myofibrillar, 9, with early respiratory failure4 tests
Myopathy, myosin storage, autosomal recessive6 tests
Myosin storage myopathy6 tests
MYPN-related myopathy6 tests
Nasopharyngeal carcinoma6 tests
Naxos disease5 tests
Neoplasm of stomach15 tests
Neuroblastoma, susceptibility to, 26 tests
Neuroblastoma, susceptibility to, 32 tests
Neurofibromatosis, type 111 tests
Neurofibromatosis, type 25 tests
Neurogenic scapuloperoneal syndrome, Kaeser type4 tests
Nijmegen breakage syndrome-like disorder4 tests
Nonpapillary renal cell carcinoma7 tests
Noonan syndrome 16 tests
Noonan syndrome 31 test
Noonan syndrome 41 test
Noonan syndrome 57 tests
Orofaciodigital syndrome I1 test
Osteosarcoma9 tests
Oto-palato-digital syndrome, type I3 tests
Oto-palato-digital syndrome, type II3 tests
Ovarian neoplasm13 tests
Pancreatic agenesis 11 test
Pancreatic cancer, susceptibility to, 213 tests
Pancreatic cancer, susceptibility to, 311 tests
Pancreatic cancer, susceptibility to, 412 tests
Paragangliomas 24 tests
Paragangliomas 34 tests
Paragangliomas 44 tests
Paragangliomas 54 tests
Paragangliomas with sensorineural hearing loss4 tests
Parkes Weber syndrome1 test
Permanent neonatal diabetes mellitus1 test
Peutz-Jeghers syndrome13 tests
PHARC syndrome1 test
Pheochromocytoma6 tests
Pilomatrixoma6 tests
Polyposis syndrome, hereditary mixed, 213 tests
Primary ciliary dyskinesia 101 test
Primary ciliary dyskinesia 111 test
Primary ciliary dyskinesia 121 test
Primary ciliary dyskinesia 131 test
Primary ciliary dyskinesia 141 test
Primary ciliary dyskinesia 151 test
Primary ciliary dyskinesia 171 test
Primary ciliary dyskinesia 181 test
Primary ciliary dyskinesia 191 test
Primary ciliary dyskinesia 21 test
Primary ciliary dyskinesia 201 test
Primary ciliary dyskinesia 231 test
Primary ciliary dyskinesia 281 test
Primary ciliary dyskinesia 31 test
Primary ciliary dyskinesia 61 test
Primary ciliary dyskinesia 71 test
Primary ciliary dyskinesia 91 test
Primary dilated cardiomyopathy1 test
Progeroid and marfanoid aspect-lipodystrophy syndrome3 tests
Progressive familial heart block type IB3 tests
Progressive familial heart block, type 1A6 tests
Prostate cancer, hereditary, 910 tests
PTEN hamartoma tumor syndrome1 test
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 12 tests
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 22 tests
Renal cell carcinoma4 tests
Renal cysts and diabetes syndrome1 test
Retinal dystrophy, reticular pigmentary, of posterior pole5 tests
Retinitis pigmentosa 231 test
Retinitis pigmentosa 31 test
Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness1 test
Retinoblastoma5 tests
Revesz syndrome1 test
Rhabdoid tumor predisposition syndrome 14 tests
Rhabdoid tumor predisposition syndrome 28 tests
Rhabdomyosarcoma, embryonal, 28 tests
Rienhoff syndrome5 tests
Rippling muscle disease4 tests
Rippling muscle disease 24 tests
Schwannomatosis1 test
Schwannomatosis 14 tests
Short QT syndrome type 14 tests
Short QT syndrome type 24 tests
Short QT syndrome type 34 tests
Shprintzen-Goldberg syndrome3 tests
Shwachman-Diamond syndrome 11 test
Sick sinus syndrome 16 tests
Sick sinus syndrome 2, autosomal dominant3 tests
Sick sinus syndrome 3, susceptibility to6 tests
Simpson-Golabi-Behmel syndrome type 21 test
Sitosterolemia1 test
Small cell lung carcinoma5 tests
Spinocerebellar ataxia type 19/223 tests
Squamous cell carcinoma of the head and neck8 tests
Stiff skin syndrome3 tests
SUDDEN INFANT DEATH SYNDROME6 tests
Surfactant metabolism dysfunction, pulmonary, 11 test
Surfactant metabolism dysfunction, pulmonary, 21 test
Telangiectasia, hereditary hemorrhagic, type 21 test
Telangiectasia, hereditary hemorrhagic, type 51 test
Terminal osseous dysplasia-pigmentary defects syndrome3 tests
Testicular anomalies with or without congenital heart disease2 tests
Tetralogy of Fallot5 tests
Tibial muscular dystrophy4 tests
Timothy syndrome4 tests
Tropical pancreatitis1 test
Trypsinogen deficiency1 test
Tuberous sclerosis 15 tests
Tuberous sclerosis 25 tests
Tumor predisposition syndrome 34 tests
Turcot syndrome7 tests
Type 1 diabetes mellitus 201 test
Type 2 diabetes mellitus1 test
VACTERL with hydrocephalus5 tests
Velocardiofacial syndrome2 tests
Ventricular fibrillation, paroxysmal familial, type 16 tests
Ventricular septal defect 12 tests
Ventricular septal defect 35 tests
Ventricular tachycardia1 test
Von Hippel-Lindau syndrome5 tests
Weill-Marchesani syndrome 2, dominant3 tests
Wilms tumor 19 tests
Wolff-Parkinson-White pattern5 tests
Woolly hair-skin fragility syndrome5 tests
X-linked cone-rod dystrophy 11 test
X-linked Emery-Dreifuss muscular dystrophy3 tests
X-linked intellectual disability with marfanoid habitus3 tests

List of services

Clinical Testing/Confirmation of Mutations Identified Previously
Confirmation of research findings
Insurance billing
Insurance preauthorization
Insurance preverification
Maternal cell contamination study (MCC)
Mutation Confirmation
Whole Exome Sequencing
Carrier Screening
Non-Invasive Prenatal Testing

List of certifications/licenses

Certifications

CLIAHelpCertification number assigned by the Clinical Laboratory Improvement Amendments (CLIA) program to the laboratory director. Minimal field for US labs offering clinical tests. Optional field for international labs or US labs performing research tests. If pending renewal or record has not been updated, the expiration date may be in the past., Number: 05D0981414, Expiration date: 2026-05-29
CAP, Number: 7154701, Expiration date: 2026-10-26

Licenses

CA - California Department of Public Health CDPH, Number: CDF00011694, Expiration date: 2025-10-17
MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 1052, Effective date: 2018-07-01 Non-expiring
NY - New York State Department of Health NYSDOH, Number: PFI: 9840, Expiration date: 2025-06-30
PA - Pennsylvania Department of Health PADOH, Number: 27832A, Expiration date: 2025-08-15
RI - State of Rhode Island Department of Health RIDOH, Number: LCO00680, Expiration date: 2025-12-30

Participation in external programs

Standardization programs

Other

Data exchange Programs

Other

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.