ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.338-20dup

dbSNP: rs370737647
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000860813 SCV001000972 benign Wilms tumor 1 2019-12-31 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257999 SCV002537453 benign Hereditary cancer-predisposing syndrome 2020-02-24 criteria provided, single submitter curation
Fulgent Genetics, Fulgent Genetics RCV002501187 SCV002804404 likely benign Wilms tumor 1; Simpson-Golabi-Behmel syndrome type 1 2022-01-06 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529337 SCV001742609 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001529337 SCV001808488 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001529337 SCV001932094 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001529337 SCV001975434 benign not specified no assertion criteria provided clinical testing

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