ClinVar Miner

Submissions for variant NM_024577.3(SH3TC2):c.73G>T (p.Asp25Tyr) (rs10066882)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000508286 SCV000605103 uncertain significance not specified 2016-09-28 criteria provided, single submitter clinical testing
Invitae RCV000471681 SCV000558064 likely benign Charcot-Marie-Tooth disease type 4 2016-12-13 criteria provided, single submitter clinical testing

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