Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001770161 | SCV002004800 | likely benign | not provided | 2018-08-14 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 15741483, 17376412, 21391883, 18192901, 19106782, 20010450, 20453482, 10768099) |