ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1680C>T (p.Ser560=)

gnomAD frequency: 0.00008  dbSNP: rs748480657
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000653762 SCV000775652 benign Wilms tumor 1 2025-01-27 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257916 SCV002537451 likely benign Hereditary cancer-predisposing syndrome 2021-05-06 criteria provided, single submitter curation

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