ClinVar Miner

Submissions for variant NM_000322.5(PRPH2):c.12G>A (p.Leu4=)

dbSNP: rs2152011167
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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 RCV001460165 SCV001664028 likely benign PRPH2-related disorder 2022-07-11 criteria provided, single submitter clinical testing

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