Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000252209 | SCV000311197 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV001089760 | SCV001941155 | benign | not provided | 2018-06-23 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001808703 | SCV002057528 | benign | Noonan syndrome 4 | 2021-07-15 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV001089760 | SCV005240012 | benign | not provided | criteria provided, single submitter | not provided | ||
Genome |
RCV001089760 | SCV001245253 | not provided | not provided | no assertion provided | phenotyping only | Variant interpreted as Benign and reported on 04-30-2009 by Lab or GTR ID 239772. GenomeConnect-CFC International assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. Registry team members make no attempt to reinterpret the clinical significance of the variant. |