ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.672A>G (p.Gln224=)

gnomAD frequency: 0.00006  dbSNP: rs373406834
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000557057 SCV000657583 likely benign Wilms tumor 1 2023-12-17 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258968 SCV002537464 uncertain significance Hereditary cancer-predisposing syndrome 2022-02-10 criteria provided, single submitter curation

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