ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.573C>T (p.Ala191=)

dbSNP: rs2124480540
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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 RCV001457215 SCV001661014 likely benign Wilms tumor 1 2020-03-05 criteria provided, single submitter clinical testing

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