ClinVar Miner

Submissions for variant NM_001386795.1(DTNA):c.93A>G (p.Arg31=)

gnomAD frequency: 0.00001  dbSNP: rs778817036
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001753031 SCV002006496 likely benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003509689 SCV004365534 benign Left ventricular noncompaction 1 2024-05-26 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005237981 SCV005883382 benign not specified 2024-12-16 criteria provided, single submitter clinical testing

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