ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.171G>A (p.Val57=)

gnomAD frequency: 0.00001  dbSNP: rs398124166
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000081104 SCV000113012 uncertain significance not provided 2013-06-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001078980 SCV000657572 benign Wilms tumor 1 2023-07-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000081104 SCV004165660 likely benign not provided 2022-10-01 criteria provided, single submitter clinical testing GPC3: BP4, BP7

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