ClinVar Miner

Submissions for variant NM_000252.3(MTM1):c.153C>T (p.Tyr51=)

dbSNP: rs2148434034
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002169104 SCV002477440 likely benign Severe X-linked myotubular myopathy 2021-05-08 criteria provided, single submitter clinical testing

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