ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1404C>T (p.His468=)

gnomAD frequency: 0.00001  dbSNP: rs145981282
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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 RCV001459017 SCV001662850 likely benign Wilms tumor 1 2022-02-05 criteria provided, single submitter clinical testing

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