ClinVar Miner

Submissions for variant NM_000322.5(PRPH2):c.657A>T (p.Pro219=)

dbSNP: rs951349581
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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 RCV001481673 SCV001686021 likely benign PRPH2-related disorder 2022-02-11 criteria provided, single submitter clinical testing

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