ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.397A>C (p.Asn133His)

gnomAD frequency: 0.00002  dbSNP: rs1339940057
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000798542 SCV000938163 likely benign Wilms tumor 1 2022-07-26 criteria provided, single submitter clinical testing

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