ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.561C>T (p.Asp187=)

dbSNP: rs921046328
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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 RCV001470996 SCV001675097 likely benign Amelocerebrohypohidrotic syndrome 2024-10-16 criteria provided, single submitter clinical testing

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