ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.297G>A (p.Glu99=)

gnomAD frequency: 0.00003  dbSNP: rs753227537
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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 RCV001460150 SCV001664013 likely benign Wilms tumor 1 2020-10-13 criteria provided, single submitter clinical testing

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