ClinVar Miner

Submissions for variant NM_152443.3(RDH12):c.907C>T (p.Leu303=)

dbSNP: rs2140162607
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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 RCV001446838 SCV001649891 likely benign Leber congenital amaurosis 13 2022-10-06 criteria provided, single submitter clinical testing

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