ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1259C>G (p.Thr420Ser)

dbSNP: rs377381100
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000463354 SCV000548709 likely benign Wilms tumor 1 2025-01-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005044679 SCV005683289 uncertain significance Wilms tumor 1; Simpson-Golabi-Behmel syndrome type 1 2024-05-08 criteria provided, single submitter clinical testing

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