ClinVar Miner

Submissions for variant NM_022455.5(NSD1):c.1338A>T (p.Ser446=)

dbSNP: rs2149842674
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003237640 SCV002011378 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003237640 SCV003238644 likely benign not provided 2022-12-10 criteria provided, single submitter clinical testing

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