ClinVar Miner

Submissions for variant NM_014391.3(ANKRD1):c.346-31_346-12del

dbSNP: rs750974250
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001547055 SCV001766677 likely benign not provided 2019-04-29 criteria provided, single submitter clinical testing
Invitae RCV002072007 SCV002410112 benign ANKRD1-related dilated cardiomyopathy 2024-01-13 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003331182 SCV004038183 benign not specified 2023-08-19 criteria provided, single submitter clinical testing

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