ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1398G>A (p.Leu466=)

gnomAD frequency: 0.00003  dbSNP: rs745968470
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000179442 SCV000231689 uncertain significance not provided 2015-03-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001079008 SCV000288567 benign Wilms tumor 1 2023-11-11 criteria provided, single submitter clinical testing

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