ClinVar Miner

Submissions for variant NM_152443.3(RDH12):c.711G>C (p.Leu237=)

dbSNP: rs766547426
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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 RCV002162243 SCV002333833 likely benign Leber congenital amaurosis 13 2021-08-23 criteria provided, single submitter clinical testing

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