ClinVar Miner

Submissions for variant NM_002470.4(MYH3):c.4324G>A (p.Ala1442Thr)

gnomAD frequency: 0.00021  dbSNP: rs201602783
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 RCV002125348 SCV002447370 likely benign not provided 2025-01-21 criteria provided, single submitter clinical testing
AiLife Diagnostics, AiLife Diagnostics RCV002125348 SCV002502155 uncertain significance not provided 2022-03-03 criteria provided, single submitter clinical testing

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