Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002173256 | SCV002350327 | likely benign | Familial cancer of breast | 2021-06-16 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV002173256 | SCV004020161 | benign | Familial cancer of breast | 2023-03-08 | criteria provided, single submitter | clinical testing | This variant is considered benign. Homozygosity for this variant has been confirmed in one or more individuals lacking clinical features consistent with gene-specific recessive disease, indicating that this variant is unlikely to be pathogenic. |