ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.338-7_338-5del

dbSNP: rs370737647
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000866619 SCV001007741 benign not provided 2017-05-17 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258010 SCV002537457 likely benign Hereditary cancer-predisposing syndrome 2022-02-03 criteria provided, single submitter curation
Fulgent Genetics, Fulgent Genetics RCV002501259 SCV002810236 likely benign Wilms tumor 1; Simpson-Golabi-Behmel syndrome type 1 2021-08-25 criteria provided, single submitter clinical testing

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