Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000917613 | SCV001062898 | benign | not provided | 2023-08-10 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003932381 | SCV004753713 | likely benign | ARHGAP31-related condition | 2019-03-05 | 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). |