Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000950079 | SCV001096359 | benign | not provided | 2023-12-18 | criteria provided, single submitter | clinical testing | |
Ce |
RCV000950079 | SCV004138688 | likely benign | not provided | 2022-05-01 | criteria provided, single submitter | clinical testing | ADCY3: BP4, BP7 |
Breakthrough Genomics, |
RCV000950079 | SCV005238922 | benign | not provided | criteria provided, single submitter | not provided | ||
Prevention |
RCV003913297 | SCV004732043 | benign | ADCY3-related disorder | 2021-09-02 | no assertion criteria provided | clinical testing | This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |