ClinVar Miner

Submissions for variant NM_000277.3(PAH):c.309T>G (p.Gly103=)

dbSNP: rs2136701573
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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 RCV002097826 SCV002383058 likely benign Phenylketonuria 2023-02-20 criteria provided, single submitter clinical testing

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