ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.889A>G (p.Arg297Gly)

gnomAD frequency: 0.00019  dbSNP: rs148951753
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000467272 SCV000559612 benign Wilms tumor 1 2025-01-22 criteria provided, single submitter clinical testing
GeneDx RCV001584186 SCV001819503 likely benign not provided 2021-02-02 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001584186 SCV004165656 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing GPC3: BP4, BS2
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001584186 SCV001931842 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001584186 SCV001972876 likely benign not provided no assertion criteria provided clinical testing

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