ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.761G>T (p.Arg254Leu)

dbSNP: rs756844729
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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 RCV000558407 SCV000657586 likely benign Wilms tumor 1 2023-12-18 criteria provided, single submitter clinical testing

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