ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1061A>G (p.Gln354Arg)

gnomAD frequency: 0.00002  dbSNP: rs1247273709
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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 RCV000814784 SCV000955210 likely benign Wilms tumor 1 2023-11-13 criteria provided, single submitter clinical testing

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