ClinVar Miner

Submissions for variant NM_002470.4(MYH3):c.375T>C (p.Thr125=)

gnomAD frequency: 0.00001  dbSNP: rs762734569
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 RCV000953948 SCV001100549 benign not provided 2024-04-15 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000953948 SCV003809553 uncertain significance not provided 2021-03-30 criteria provided, single submitter clinical testing

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