ClinVar Miner

Submissions for variant NM_018328.4(MBD5):c.4158C>T (p.Gly1386=) (rs543329958)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000192328 SCV000247912 uncertain significance not specified 2014-10-24 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000765519 SCV000896829 uncertain significance Mental retardation, autosomal dominant 1 2018-10-31 criteria provided, single submitter clinical testing
Invitae RCV000765519 SCV001007147 likely benign Mental retardation, autosomal dominant 1 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000866097 SCV001144477 likely benign not provided 2019-07-03 criteria provided, single submitter clinical testing

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