GeneID Lab - Advanced Molecular Diagnostics
General information
GeneID Lab - Advanced Molecular Diagnostics
Montvale
New Jersey
United States
http://www.geneidlab.com
Organization ID: 506582
Montvale
New Jersey
United States
http://www.geneidlab.com
Organization ID: 506582
Assertion criteria
Level: Assertion criteria provided
Summary of submissions to ClinVar
Total submissions: 48
Gene
Gene | Submissions | Last Updated |
---|---|---|
AKAP9 | 1 | Jul 16, 2018 |
BCKDHB | 2 | Nov 4, 2021 |
BLM | 1 | Nov 4, 2021 |
BRCA2 | 1 | Nov 4, 2021 |
BRIP1 | 1 | Sep 11, 2017 |
CA12 | 1 | Jul 16, 2018 |
CDH1 | 1 | Sep 11, 2017 |
CDH23 | 2 | Nov 4, 2021 |
CHEK2 | 1 | Sep 11, 2017 |
COL4A1 | 1 | Nov 4, 2021 |
ELAC2 | 1 | Nov 4, 2021 |
ELP1 | 1 | Jul 16, 2018 |
FANCA | 1 | Nov 4, 2021 |
GBA1 | 2 | Nov 4, 2021 |
GBE1 | 1 | Jul 16, 2018 |
GJB2 | 1 | Nov 4, 2021 |
GJB3 | 1 | Jul 16, 2018 |
GJB6 | 2 | Jul 16, 2018 |
HEXA | 2 | Nov 4, 2021 |
LOC106627981 | 2 | Nov 4, 2021 |
MSH6 | 3 | Nov 4, 2021 |
MUTYH | 1 | Sep 11, 2017 |
MYO7A | 2 | Nov 4, 2021 |
NBN | 3 | Nov 4, 2021 |
PAH | 1 | Sep 11, 2017 |
PALB2 | 1 | Nov 4, 2021 |
PCDH15 | 3 | Jul 16, 2018 |
PTCH1 | 1 | Nov 4, 2021 |
RAD50 | 1 | Nov 4, 2021 |
RECQL4 | 2 | Nov 4, 2021 |
SCN5A | 1 | Nov 4, 2021 |
SCNN1B | 1 | Jul 16, 2018 |
TGFBR2 | 1 | Jul 16, 2018 |
USH2A | 3 | Jul 16, 2018 |
USH2A-AS2 | 1 | Sep 11, 2017 |
Condition
Testing in GTR
Disease name | Number of tests |
---|---|
Acute lymphoid leukemia | 1 test |
Adult-onset proximal spinal muscular atrophy, autosomal dominant | 1 test |
Amyotrophic lateral sclerosis type 8 | 1 test |
Aneurysm-osteoarthritis syndrome | 1 test |
Aortic aneurysm, familial thoracic 4 | 1 test |
Aortic aneurysm, familial thoracic 6 | 1 test |
Aortic aneurysm, familial thoracic 7 | 1 test |
Aplastic anemia | 2 tests |
Arterial tortuosity syndrome | 1 test |
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures | 1 test |
Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome | 1 test |
Autosomal dominant nonsyndromic hearing loss 13 | 1 test |
Autosomal dominant nonsyndromic hearing loss 2A | 1 test |
Autosomal dominant nonsyndromic hearing loss 2B | 1 test |
Autosomal dominant nonsyndromic hearing loss 3A | 1 test |
Autosomal dominant nonsyndromic hearing loss 3B | 1 test |
Autosomal recessive nonsyndromic hearing loss 1A | 1 test |
BAP1-related tumor predisposition syndrome | 2 tests |
Baller-Gerold syndrome | 1 test |
Bannayan-Riley-Ruvalcaba syndrome | 2 tests |
Basal cell carcinoma, somatic | 1 test |
Bloom syndrome | 1 test |
Breast and colorectal cancer, susceptibility to | 3 tests |
Breast lobular carcinoma | 2 tests |
Breast-ovarian cancer, familial, susceptibility to, 1 | 4 tests |
Breast-ovarian cancer, familial, susceptibility to, 2 | 3 tests |
Breast-ovarian cancer, familial, susceptibility to, 3 | 2 tests |
Breast-ovarian cancer, familial, susceptibility to, 4 | 2 tests |
Bronchiectasis with or without elevated sweat chloride 1 | 1 test |
Bronchiectasis with or without elevated sweat chloride 2 | 1 test |
Bronchiectasis with or without elevated sweat chloride 3 | 1 test |
Canavan Disease, Familial Form | 1 test |
Carcinoma of colon | 1 test |
Carcinoma of pancreas | 1 test |
Colorectal cancer, hereditary nonpolyposis, type 2 | 4 tests |
Colorectal cancer, susceptibility to | 2 tests |
Colorectal cancer, susceptibility to, 10 | 2 tests |
Colorectal cancer, susceptibility to, 12 | 2 tests |
Cowden syndrome 1 | 2 tests |
Cystic fibrosis | 1 test |
Decreased activity of the pyruvate dehydrogenase complex | 1 test |
Ehlers-Danlos syndrome, type 4 | 1 test |
Endometrial carcinoma | 1 test |
Familial adenomatous polyposis 1 | 2 tests |
Familial adenomatous polyposis 2 | 2 tests |
Familial cancer of breast | 2 tests |
Familial colorectal cancer | 3 tests |
Familial dysautonomia | 1 test |
Familial melanoma | 2 tests |
Familial pancreatic carcinoma | 1 test |
Familial thoracic aortic aneurysm and aortic dissection | 1 test |
Fanconi anemia complementation group A | 1 test |
Fanconi anemia complementation group C | 1 test |
Fanconi anemia complementation group F | 1 test |
Fanconi anemia complementation group G | 1 test |
Fanconi anemia complementation group O | 2 tests |
Fragile X syndrome | 1 test |
Galactosemia | 1 test |
Gaucher disease | 1 test |
Generalized juvenile polyposis/juvenile polyposis coli | 2 tests |
Glycogen storage disease, type II | 1 test |
Glycogen storage disease, type IV | 1 test |
Gorlin syndrome | 1 test |
Hb SS disease | 1 test |
Hereditary breast ovarian cancer syndrome | 4 tests |
Hereditary cancer-predisposing syndrome | 4 tests |
Hereditary diffuse gastric adenocarcinoma | 2 tests |
Hereditary nonpolyposis colon cancer | 1 test |
Infantile-onset X-linked spinal muscular atrophy | 1 test |
Isolated hyperchlorhidrosis | 1 test |
Jervell and Lange-Nielsen syndrome 1 | 1 test |
Jervell and Lange-Nielsen syndrome 2 | 1 test |
Juvenile Polyposis | 1 test |
Leukemia, acute lymphoblastic, susceptibility to | 1 test |
Li-Fraumeni syndrome 1 | 3 tests |
Li-Fraumeni syndrome 2 | 3 tests |
Liddle syndrome 1 | 1 test |
Liddle syndrome 2 | 1 test |
Liddle syndrome 3 | 1 test |
Loeys-Dietz syndrome 1 | 1 test |
Loeys-Dietz syndrome 2 | 1 test |
Long QT syndrome 1 | 1 test |
Long QT syndrome 11 | 1 test |
Long QT syndrome 3 | 1 test |
Long QT syndrome 5 | 1 test |
Long QT syndrome 6 | 1 test |
Lung adenocarcinoma | 1 test |
Lymphoma, non-Hodgkin, familial | 1 test |
Lynch syndrome | 2 tests |
Lynch syndrome 1 | 4 tests |
Lynch syndrome 4 | 4 tests |
Lynch syndrome 5 | 4 tests |
Lynch syndrome 8 | 3 tests |
Malignant melanoma of skin | 1 test |
Malignant tumor of breast | 1 test |
Malignant tumor of prostate | 1 test |
Maple syrup urine disease type 1A | 1 test |
Maple syrup urine disease type 1B | 1 test |
Maple syrup urine disease type 2 | 1 test |
Marfan syndrome | 1 test |
Melanoma, cutaneous malignant, susceptibility to, 2 | 2 tests |
Melanoma, cutaneous malignant, susceptibility to, 3 | 1 test |
Melanoma-pancreatic cancer syndrome | 2 tests |
Mismatch repair cancer syndrome 1 | 4 tests |
Mucolipidosis type IV | 1 test |
Muir-Torré syndrome | 2 tests |
Multiple endocrine neoplasia type 2A | 1 test |
Multiple endocrine neoplasia type 2B | 1 test |
Multiple myeloma | 1 test |
Neoplasm | 2 tests |
Neoplasm of the large intestine | 1 test |
Niemann-Pick disease, type C1 | 1 test |
Niemann-Pick disease, type C2 | 1 test |
Nijmegen breakage syndrome-like disorder | 1 test |
Non-Hodgkin lymphoma | 2 tests |
Ornithine carbamoyltransferase deficiency | 1 test |
PTEN hamartoma tumor syndrome | 2 tests |
Pancreatic cancer, susceptibility to, 2 | 1 test |
Pancreatic cancer, susceptibility to, 3 | 2 tests |
Pancreatic cancer, susceptibility to, 4 | 2 tests |
Papillary renal cell carcinoma type 1 | 2 tests |
Pendred syndrome | 1 test |
Peutz-Jeghers syndrome | 2 tests |
Phenylketonuria | 1 test |
Pheochromocytoma | 1 test |
Polyposis syndrome, hereditary mixed, 1 | 1 test |
Prostate cancer susceptibility | 2 tests |
Prostate cancer, hereditary, 2 | 2 tests |
Proteus syndrome | 2 tests |
Proteus-like syndrome | 2 tests |
Pseudohypoaldosteronism, type IB1, autosomal recessive | 1 test |
Pyruvate dehydrogenase E3 deficiency | 1 test |
Rapadilino syndrome | 1 test |
Renal cell carcinoma | 1 test |
Rothmund-Thomson syndrome | 1 test |
Spinal muscular atrophy | 1 test |
Tay-Sachs disease | 1 test |
Usher Syndrome, Type 1A | 1 test |
Usher syndrome type 1 | 1 test |
Usher syndrome type 1B | 1 test |
Usher syndrome type 1C | 1 test |
Usher syndrome type 1D | 1 test |
Usher syndrome type 1F | 1 test |
Usher syndrome type 2A | 1 test |
Werdnig-Hoffmann disease | 1 test |
alpha Thalassemia | 1 test |
beta Thalassemia | 1 test |