ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1601A>G (p.Asp534Gly)

gnomAD frequency: 0.00004  dbSNP: rs755823884
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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 RCV001453749 SCV001657449 likely benign Wilms tumor 1 2021-09-03 criteria provided, single submitter clinical testing

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