Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000220626 | SCV000268862 | benign | not specified | 2015-04-16 | criteria provided, single submitter | clinical testing | p.Glu118Lys in exon 3 of CEACAM16: This variant is not expected to have clinical significance because it has been identified in 0.5% (188/34916) of European chr omosomes including 1 homozygote by the Exome Aggregation Consortium (ExAC, http: //exac.broadinstitute.org; dbSNP rs183860695). |
Prevention |
RCV000220626 | SCV000306125 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Eurofins Ntd Llc |
RCV000220626 | SCV000705005 | benign | not specified | 2017-01-17 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000963022 | SCV000732297 | benign | not provided | 2018-09-28 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000963022 | SCV001110148 | benign | not provided | 2023-12-25 | criteria provided, single submitter | clinical testing |