Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
OMIM | RCV000578209 | SCV000680079 | pathogenic | SLC35A1-congenital disorder of glycosylation | 2018-02-01 | no assertion criteria provided | literature only | |
University of Washington Center for Mendelian Genomics, |
RCV000578209 | SCV001197905 | likely pathogenic | SLC35A1-congenital disorder of glycosylation | no assertion criteria provided | research |