ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.844A>G (p.Met282Val)

gnomAD frequency: 0.00001  dbSNP: rs151082475
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000525913 SCV000657589 benign Wilms tumor 1 2024-05-21 criteria provided, single submitter clinical testing
GeneDx RCV001568273 SCV001792115 likely benign not provided 2020-11-30 criteria provided, single submitter clinical testing

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