ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.459T>G (p.Ser153=)

gnomAD frequency: 0.00005  dbSNP: rs775459305
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001513296 SCV001720889 benign Wilms tumor 1 2024-05-09 criteria provided, single submitter clinical testing

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