ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.3946G>A (p.Asp1316Asn)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003333546 SCV004041207 uncertain significance MYH6-related cardiac defects 2023-04-10 criteria provided, single submitter clinical testing
Baylor Genetics RCV003333545 SCV004041337 uncertain significance Dilated cardiomyopathy 1EE 2023-04-10 criteria provided, single submitter clinical testing
Baylor Genetics RCV003333544 SCV004041552 uncertain significance Atrial septal defect 3 2023-04-10 criteria provided, single submitter clinical testing

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