ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1078G>T (p.Ala360Ser)

gnomAD frequency: 0.00005  dbSNP: rs779187915
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000819371 SCV000960026 likely benign Wilms tumor 1 2023-08-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003437439 SCV004165653 uncertain significance not provided 2022-08-01 criteria provided, single submitter clinical testing

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