ClinVar Miner

Submissions for variant NM_001353214.3(DYM):c.2026-5T>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002797837 SCV003586332 uncertain significance Inborn genetic diseases 2021-12-21 criteria provided, single submitter clinical testing The c.1861-5T>C intronic alteration consists of a T to C substitution 5 nucleotides before coding exon 16 in the DYM gene. Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
Labcorp Genetics (formerly Invitae), Labcorp RCV003777759 SCV004682305 likely benign not provided 2023-03-31 criteria provided, single submitter clinical testing

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