Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000036834 | SCV000060489 | benign | not specified | 2012-04-30 | criteria provided, single submitter | clinical testing | Val2300Ala in Exon 22 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 1.8% (60/3292) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://evs.gs.washington.edu/EVS; dbSNP rs61737841). |
Prevention |
RCV000036834 | SCV000306119 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV000840104 | SCV000982020 | benign | not provided | 2019-05-16 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000840104 | SCV001031890 | benign | not provided | 2024-01-18 | criteria provided, single submitter | clinical testing |