ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.852C>T (p.Gly284=)

dbSNP: rs1603240522
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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 RCV001460049 SCV001663910 likely benign Wilms tumor 1 2022-11-29 criteria provided, single submitter clinical testing

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