ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.18A>G (p.Ala6=)

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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 RCV003646055 SCV004382272 likely benign Amelocerebrohypohidrotic syndrome 2023-11-29 criteria provided, single submitter clinical testing

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