ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.2307G>T (p.Leu769=)

dbSNP: rs2502286230
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004015223 SCV004827989 likely benign Cardiomyopathy 2023-08-28 criteria provided, single submitter clinical testing

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