ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.357T>C (p.His119=)

dbSNP: rs2082694921
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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 RCV002192734 SCV002351792 likely benign Amelocerebrohypohidrotic syndrome 2025-01-19 criteria provided, single submitter clinical testing

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