ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.93G>A (p.Pro31=)

gnomAD frequency: 0.00007  dbSNP: rs781232455
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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 RCV000470462 SCV000548713 likely benign Wilms tumor 1 2024-01-15 criteria provided, single submitter clinical testing

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