ClinVar Miner

Submissions for variant NM_013266.4(CTNNA3):c.99+11C>T

gnomAD frequency: 0.00411  dbSNP: rs115451937
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002077135 SCV002466019 benign Arrhythmogenic right ventricular dysplasia 13 2025-01-30 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001700888 SCV004804282 benign not specified 2024-01-08 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700888 SCV001919074 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001700887 SCV001926500 likely benign not provided no assertion criteria provided clinical testing

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