ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.326C>T (p.Ala109Val)

dbSNP: rs761660909
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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 RCV000701104 SCV000829887 benign Wilms tumor 1 2022-11-23 criteria provided, single submitter clinical testing

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