ClinVar Miner

Submissions for variant NM_020884.7(MYH7B):c.4119C>T (p.Ala1373=)

gnomAD frequency: 0.04770  dbSNP: rs17092206
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 RCV002164413 SCV002477881 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002164413 SCV005315650 benign not provided criteria provided, single submitter not provided

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