ClinVar Miner

Submissions for variant NM_014391.3(ANKRD1):c.346-21_346-12del

dbSNP: rs796121587
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002105952 SCV002405223 likely benign ANKRD1-related dilated cardiomyopathy 2025-02-02 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003923622 SCV004745810 likely benign ANKRD1-related disorder 2021-07-01 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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