Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000221957 | SCV000269913 | benign | not specified | 2012-04-30 | criteria provided, single submitter | clinical testing | Asn2269Ser in Exon 21 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 1.6% (54/3292) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://evs.gs.washington.edu/EVS; dbSNP rs61729060). |
Prevention |
RCV000221957 | SCV000306118 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV000905231 | SCV000727305 | benign | not provided | 2019-02-26 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000905231 | SCV001049801 | benign | not provided | 2024-01-29 | criteria provided, single submitter | clinical testing |