ClinVar Miner

Submissions for variant NM_005660.3(SLC35A2):c.92-7C>G

gnomAD frequency: 0.00001  dbSNP: rs1557043678
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000999419 SCV001156027 uncertain significance not provided 2016-06-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001450426 SCV001654033 likely benign SLC35A2-congenital disorder of glycosylation 2024-10-17 criteria provided, single submitter clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV000999419 SCV002011198 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing

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