ClinVar Miner

Submissions for variant NM_152443.3(RDH12):c.693C>A (p.Gly231=)

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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 RCV005117746 SCV005737171 likely benign Leber congenital amaurosis 13 2024-02-02 criteria provided, single submitter clinical testing

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