ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.942T>C (p.Tyr314=)

dbSNP: rs1603240471
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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 RCV000867850 SCV001009120 likely benign Wilms tumor 1 2021-06-19 criteria provided, single submitter clinical testing

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