ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.392A>G (p.Lys131Arg)

gnomAD frequency: 0.00001  dbSNP: rs751302717
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000231451 SCV000288575 benign Wilms tumor 1 2024-07-21 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001572876 SCV001797924 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001572876 SCV001970396 uncertain significance not provided no assertion criteria provided clinical testing

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