Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000968798 | SCV001116272 | benign | not provided | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002503055 | SCV002805804 | likely benign | Lymphatic malformation 9 | 2021-12-03 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV000968798 | SCV005275728 | benign | not provided | criteria provided, single submitter | not provided | ||
Prevention |
RCV003916267 | SCV004734150 | benign | CELSR1-related disorder | 2019-11-11 | no assertion criteria provided | clinical testing | This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |