ClinVar Miner

Submissions for variant NM_002473.6(MYH9):c.108C>T (p.Ser36=)

gnomAD frequency: 0.00002  dbSNP: rs764743124
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000734683 SCV000862842 uncertain significance not provided 2018-08-17 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000734683 SCV004703624 likely benign not provided 2024-02-01 criteria provided, single submitter clinical testing MYH9: BP4, BP7

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