ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.165C>G (p.Pro55=)

dbSNP: rs1455879564
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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 RCV001472679 SCV001676815 likely benign Amelocerebrohypohidrotic syndrome 2020-07-01 criteria provided, single submitter clinical testing

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