Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000911335 | SCV001056400 | benign | not provided | 2024-01-03 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003902889 | SCV004727040 | likely benign | LAMA5-related disorder | 2020-01-03 | 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). |