ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.175+12T>G

gnomAD frequency: 0.00002  dbSNP: rs765877667
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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 RCV002200587 SCV002482186 likely benign Wilms tumor 1 2023-11-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486992 SCV002804223 likely benign Wilms tumor 1; Simpson-Golabi-Behmel syndrome type 1 2022-05-08 criteria provided, single submitter clinical testing

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