Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001712207 | SCV000516152 | likely benign | not provided | 2021-05-20 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000546560 | SCV000651803 | likely benign | Pitt-Hopkins-like syndrome 2 | 2023-12-08 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002446662 | SCV002732057 | likely benign | Inborn genetic diseases | 2017-12-15 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |