ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.687C>T (p.Phe229=)

dbSNP: rs2124480310
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001463948 SCV001667904 likely benign Wilms tumor 1 2022-01-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003438811 SCV004165658 likely benign not provided 2023-05-01 criteria provided, single submitter clinical testing GPC3: PM2:Supporting, BP4, BP7

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