ClinVar Miner

Submissions for variant NM_005428.4(VAV1):c.1980T>C (p.His660=)

gnomAD frequency: 0.00662  dbSNP: rs112350637
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000954168 SCV001100782 benign not provided 2024-01-30 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000954168 SCV001159120 benign not provided 2023-09-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000954168 SCV002498410 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing VAV1: BP4, BP7, BS2

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