ClinVar Miner

Submissions for variant NM_014391.3(ANKRD1):c.345+17dup

dbSNP: rs746808032
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002075263 SCV002374970 benign ANKRD1-related dilated cardiomyopathy 2023-12-23 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003331290 SCV004038184 benign not specified 2023-08-19 criteria provided, single submitter clinical testing

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