Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000470132 | SCV000557460 | likely benign | Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome | 2023-12-12 | criteria provided, single submitter | clinical testing | |
Ce |
RCV003884556 | SCV004699595 | likely benign | not provided | 2023-12-01 | criteria provided, single submitter | clinical testing | WT1: BP4, BP7 |
Prevention |
RCV003970313 | SCV004788752 | likely benign | WT1-related condition | 2019-02-19 | 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). |