ClinVar Miner

Submissions for variant NM_000277.3(PAH):c.921C>T (p.Gly307=)

dbSNP: rs920882128
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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 RCV001415115 SCV001617264 likely benign Phenylketonuria 2022-03-31 criteria provided, single submitter clinical testing

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