ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.96G>A (p.Lys32=)

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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 RCV002642427 SCV002964691 likely benign Amelocerebrohypohidrotic syndrome 2022-03-02 criteria provided, single submitter clinical testing

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