SCV000885053 | ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories | criteria provided, single submitter (ARUP Molecular Germline Variant Investigation Process 2024) | Uncertain significance
(Nov 21, 2023)
| germline | clinical testing | Citation Link, |
SCV000894839 | Fulgent Genetics, Fulgent Genetics | criteria provided, single submitter (ACMG Guidelines, 2015) | Uncertain significance
(Oct 31, 2018)
| unknown | clinical testing | PubMed (1) [See all records that cite this PMID] |
SCV001016601 | Invitae | criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) | Likely benign
(Jan 31, 2024)
| germline | clinical testing | PubMed (1) [See all records that cite this PMID] |
SCV001139346 | Mendelics | criteria provided, single submitter (Mendelics Assertion Criteria 2017) | Uncertain significance
(May 28, 2019)
| unknown | clinical testing | Citation Link, |
SCV001267651 | Illumina Laboratory Services, Illumina | criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019) | Uncertain significance
(Feb 20, 2018)
| germline | clinical testing | PubMed (4) [See all records that cite these PMIDs] Citation Link, |
SCV001466729 | Natera, Inc. | no assertion criteria provided | Benign
(Oct 8, 2020)
| germline | clinical testing | |
SCV001977530 | Genome-Nilou Lab | criteria provided, single submitter (ACMG Guidelines, 2015) | Uncertain significance
(Aug 10, 2021)
| germline | clinical testing | PubMed (1) [See all records that cite this PMID] |
SCV002028338 | Centogene AG - the Rare Disease Company | criteria provided, single submitter (ACMG Guidelines, 2015) | Uncertain significance
(Mar 24, 2017)
| germline | clinical testing | PubMed (1) [See all records that cite this PMID] |
SCV004361952 | Color Diagnostics, LLC DBA Color Health | criteria provided, single submitter (ACMG Guidelines, 2015) | Uncertain significance
(Dec 12, 2022)
| germline | clinical testing | PubMed (6) [See all records that cite these PMIDs] |