ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.365C>T (p.Ala122Val)

gnomAD frequency: 0.00003  dbSNP: rs779679730
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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 RCV000870430 SCV001011927 benign Wilms tumor 1 2024-11-13 criteria provided, single submitter clinical testing
GeneDx RCV001548625 SCV001768569 likely benign not provided 2020-10-13 criteria provided, single submitter clinical testing

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