ClinVar Miner

Submissions for variant NM_002473.6(MYH9):c.72C>T (p.Ala24=)

gnomAD frequency: 0.00005  dbSNP: rs756727165
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001544791 SCV001763990 likely benign not provided 2020-10-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001544791 SCV005825267 likely benign not provided 2024-10-25 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001544791 SCV005876713 likely benign not provided 2023-12-11 criteria provided, single submitter clinical testing

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