ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1437C>G (p.Pro479=)

gnomAD frequency: 0.00001  dbSNP: rs1337307928
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 RCV001461692 SCV001665598 likely benign Wilms tumor 1 2023-02-10 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003438553 SCV004165649 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing GPC3: BP4, BP7

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