ClinVar Miner

Submissions for variant NM_152443.3(RDH12):c.659-10T>C

gnomAD frequency: 0.00001  dbSNP: rs754817805
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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 RCV001401044 SCV001602858 likely benign Leber congenital amaurosis 13 2023-08-18 criteria provided, single submitter clinical testing

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