ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.1002+1G>T

dbSNP: rs776627067
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
AiLife Diagnostics, AiLife Diagnostics RCV002224468 SCV002503177 uncertain significance not provided 2021-12-23 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502039 SCV002793188 uncertain significance Hypertrophic cardiomyopathy 1; Dilated cardiomyopathy 1EE; Hypertrophic cardiomyopathy 14; Atrial septal defect 3; Sick sinus syndrome 3, susceptibility to 2021-10-13 criteria provided, single submitter clinical testing

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