ClinVar Miner

Submissions for variant NM_000322.5(PRPH2):c.564C>T (p.Ser188=)

dbSNP: rs1398721260
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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 RCV002071091 SCV002323484 likely benign PRPH2-related disorder 2022-07-12 criteria provided, single submitter clinical testing

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