ClinVar Miner

Submissions for variant NM_058179.4(PSAT1):c.726G>T (p.Thr242=)

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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 RCV002609360 SCV002959319 likely benign Neu-Laxova syndrome 2 2022-05-05 criteria provided, single submitter clinical testing

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