ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.342C>T (p.Ala114=)

gnomAD frequency: 0.00001  dbSNP: rs748391795
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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 RCV001422383 SCV001624929 likely benign Wilms tumor 1 2023-10-30 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258242 SCV002537458 likely benign Hereditary cancer-predisposing syndrome 2021-10-15 criteria provided, single submitter curation

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