ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1114G>A (p.Val372Ile)

gnomAD frequency: 0.00002  dbSNP: rs140756498
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000543927 SCV000657559 likely benign Wilms tumor 1 2024-01-07 criteria provided, single submitter clinical testing
GeneDx RCV001796124 SCV002032803 likely benign not provided 2021-02-08 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV001796124 SCV002541765 uncertain significance not provided 2021-07-23 criteria provided, single submitter clinical testing

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