Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000822970 | SCV000963802 | likely benign | RASopathy | 2023-12-19 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV001174908 | SCV001338340 | likely benign | not specified | 2020-02-29 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003955533 | SCV004768363 | likely benign | SOS1-related disorder | 2022-01-07 | no assertion criteria provided | clinical testing | This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |