ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1725C>T (p.Phe575=)

dbSNP: rs925042479
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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 RCV001400788 SCV001602598 likely benign Wilms tumor 1 2022-10-21 criteria provided, single submitter clinical testing

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