ClinVar Miner

Submissions for variant NM_000277.3(PAH):c.783A>G (p.Arg261=)

dbSNP: rs2136646206
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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 RCV001439645 SCV001642537 likely benign Phenylketonuria 2019-08-19 criteria provided, single submitter clinical testing

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