ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.309G>C (p.Arg103=)

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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 RCV003042582 SCV003332600 likely benign Amelocerebrohypohidrotic syndrome 2022-03-18 criteria provided, single submitter clinical testing

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