ClinVar Miner

Submissions for variant NM_138425.4(C12orf57):c.319C>T (p.Leu107=)

dbSNP: rs374912364
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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 RCV001403461 SCV001605332 likely benign Temtamy syndrome 2024-02-24 criteria provided, single submitter clinical testing

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