ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1011T>C (p.Asn337=)

dbSNP: rs2124479734
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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 RCV001423497 SCV001626078 likely benign Wilms tumor 1 2019-03-13 criteria provided, single submitter clinical testing

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