Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000370604 | SCV000336445 | benign | not specified | 2015-10-26 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000370604 | SCV000518120 | likely benign | not specified | 2016-06-22 | 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 | RCV000560916 | SCV000648311 | benign | Congenital muscular dystrophy due to integrin alpha-7 deficiency | 2024-01-29 | criteria provided, single submitter | clinical testing | |
Ce |
RCV003389778 | SCV004133433 | benign | not provided | 2023-09-01 | criteria provided, single submitter | clinical testing | ITGA7: BS1, BS2 |