ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.201+17G>A

gnomAD frequency: 0.00002  dbSNP: rs374935099
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002113196 SCV002408583 likely benign Hypertrophic cardiomyopathy 14 2024-07-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706346 SCV005211398 likely benign not provided criteria provided, single submitter not provided

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