ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1178A>C (p.Gln393Pro)

gnomAD frequency: 0.00001  dbSNP: rs1313616176
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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 RCV001036985 SCV001200376 likely benign Wilms tumor 1 2023-11-17 criteria provided, single submitter clinical testing

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