ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.802C>T (p.Leu268=)

gnomAD frequency: 0.00001  dbSNP: rs754903885
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698054 SCV000728245 likely benign not provided 2020-11-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000937747 SCV001083538 likely benign Wilms tumor 1 2023-06-17 criteria provided, single submitter clinical testing

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