Clinical Genomics Laboratory (Laboratory for Precision Diagnostics, University of Washington)
General information
Clinical Genomics Laboratory
Laboratory for Precision Diagnostics, University of Washington
1959 NE Pacific St., HSB H-561
Seattle
Washington
United States - 98195
http://uwcpdx.org/clinical-genomics-laboratory/
Organization ID: 505820
Laboratory for Precision Diagnostics, University of Washington
1959 NE Pacific St., HSB H-561
Seattle
Washington
United States - 98195
http://uwcpdx.org/clinical-genomics-laboratory/
Organization ID: 505820
Assertion criteria
Level: Assertion criteria provided
Summary of submissions to ClinVar
Total submissions: 422
Gene
| Gene | Submissions | Last Updated |
|---|---|---|
| ASTN2 | 1 | Nov 15, 2018 |
| AUTS2 | 1 | Aug 2, 2017 |
| BRCA1 | 1 | Jan 8, 2026 |
| CNTN4 | 2 | Mar 19, 2020 |
| CREBBP | 1 | Mar 29, 2017 |
| CSMD1 | 1 | Aug 2, 2017 |
| DCC | 1 | Jan 8, 2026 |
| DMD | 1 | Jan 8, 2026 |
| EYA1 | 1 | Mar 29, 2017 |
| FAF1 | 1 | May 8, 2019 |
| FOXP1 | 1 | Aug 2, 2017 |
| GPC5 | 1 | Jan 22, 2016 |
| LRP1B | 1 | May 8, 2019 |
| MARCHF1 | 1 | Apr 4, 2016 |
| MBD5 | 1 | Jan 26, 2018 |
| MED13L | 1 | Nov 15, 2018 |
| NR2F2 | 1 | Aug 2, 2017 |
| NR3C2 | 1 | Jan 22, 2016 |
| NRG3 | 1 | Apr 4, 2016 |
| PPP3CA | 1 | May 8, 2019 |
| PRICKLE1 | 1 | Mar 19, 2020 |
| PRKN | 2 | Nov 22, 2017 |
| PTPRN2 | 1 | May 8, 2019 |
| SLC3A1 | 1 | Apr 4, 2016 |
| TCF12 | 1 | May 8, 2019 |
Condition
| Name | Submissions | Last Updated |
|---|---|---|
| See cases | 418 | Jan 8, 2026 |
| not provided | 2 | Apr 4, 2016 |
| not specified | 2 | Apr 4, 2016 |
Testing in GTR
| Disease name | Number of tests |
|---|---|
| 17p11.2 microduplication syndrome | 1 test |
| 4p partial monosomy syndrome | 1 test |
| 5p partial monosomy syndrome | 1 test |
| 7q11.23 microduplication syndrome | 1 test |
| Acute lymphoid leukemia | 2 tests |
| Acute myeloid leukemia | 2 tests |
| Advanced maternal age gravida | 1 test |
| Angelman syndrome | 1 test |
| Autism spectrum disorder | 1 test |
| B-cell chronic lymphocytic leukemia | 2 tests |
| B-cell non-Hodgkin lymphoma | 2 tests |
| Chromophobe renal cell carcinoma | 1 test |
| Chromosome 15q11.2 duplication syndrome | 1 test |
| Chromosome 1p36 deletion syndrome | 1 test |
| Chromosome 22q11.2 deletion syndrome, distal | 1 test |
| Chromosome 22q11.2 microduplication syndrome | 1 test |
| Clear cell carcinoma of kidney | 1 test |
| Cognitive impairment | 1 test |
| Congenital chromosomal disease | 1 test |
| Dysmorphic features | 1 test |
| Glioblastoma | 2 tests |
| Hematologic neoplasm | 1 test |
| Hypogonadism with anosmia | 1 test |
| Intellectual disability | 1 test |
| Known OR suspected fetal abnormality affecting management of mother | 1 test |
| Lung carcinoma | 1 test |
| Lymphoid leukemia | 1 test |
| Lymphoma | 2 tests |
| Maternal care for suspected chromosomal abnormality in fetus | 1 test |
| Miller Dieker syndrome | 1 test |
| Miscarriage | 1 test |
| Multiple congenital anomalies | 1 test |
| Multiple myeloma | 3 tests |
| Myelodysplastic syndrome | 2 tests |
| Myeloid leukemia | 1 test |
| Nonpapillary renal cell carcinoma | 1 test |
| Pallister-Killian syndrome | 1 test |
| Papillary renal cell carcinoma | 1 test |
| Partial autosomal deletion | 1 test |
| Plasma cell neoplasm | 1 test |
| Prader-Willi syndrome | 1 test |
| Renal cell carcinoma | 2 tests |
| Sarcoma | 2 tests |
| Smith-Magenis syndrome | 1 test |
| Solid tumor | 3 tests |
| Velocardiofacial syndrome | 1 test |
| Williams syndrome | 1 test |
| X-linked ichthyosis with steryl-sulfatase deficiency | 1 test |