Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000725949 | SCV000340765 | uncertain significance | not provided | 2016-03-25 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000390756 | SCV000718581 | likely benign | not specified | 2017-04-12 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Invitae | RCV001276777 | SCV001671065 | likely benign | Autosomal recessive polycystic kidney disease | 2023-09-01 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001276777 | SCV001463305 | likely benign | Autosomal recessive polycystic kidney disease | 2020-09-16 | no assertion criteria provided | clinical testing |