ClinVar Miner

Submissions for variant NM_152443.3(RDH12):c.828C>G (p.Pro276=)

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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 RCV002800603 SCV003033200 likely benign Leber congenital amaurosis 13 2022-06-08 criteria provided, single submitter clinical testing

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