ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.117+10C>T

dbSNP: rs113858060
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001082742 SCV000561649 benign Amelocerebrohypohidrotic syndrome 2025-02-02 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000712936 SCV000843494 benign not provided 2017-11-20 criteria provided, single submitter clinical testing

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