ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.777C>T (p.Val259=)

dbSNP: rs372599256
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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 RCV001448807 SCV001651908 likely benign Amelocerebrohypohidrotic syndrome 2023-06-29 criteria provided, single submitter clinical testing

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