Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000343047 | SCV000336187 | benign | not specified | 2015-10-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001705416 | SCV000524181 | likely benign | not provided | 2020-03-15 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001705416 | SCV002421132 | benign | not provided | 2024-01-19 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003939982 | SCV004752714 | likely benign | LAMC3-related condition | 2019-06-28 | criteria provided, single submitter | 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). |