ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.633C>T (p.Phe211=)

dbSNP: rs2071696918
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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 RCV001457470 SCV001661273 likely benign Wilms tumor 1 2024-01-17 criteria provided, single submitter clinical testing

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