ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.450A>G (p.Thr150=)

gnomAD frequency: 0.00001  dbSNP: rs1569426383
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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 RCV002119721 SCV002396537 likely benign Wilms tumor 1 2021-12-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507983 SCV002806328 likely benign Wilms tumor 1; Simpson-Golabi-Behmel syndrome type 1 2021-10-28 criteria provided, single submitter clinical testing

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