ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.825C>T (p.Gly275=)

gnomAD frequency: 0.00006  dbSNP: rs753811089
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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 RCV001513458 SCV001721076 benign Wilms tumor 1 2024-09-08 criteria provided, single submitter clinical testing

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