ClinVar Miner

Submissions for variant NM_014915.3(ANKRD26):c.303C>G (p.Asp101Glu)

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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 RCV003719950 SCV004512001 benign not provided 2024-01-05 criteria provided, single submitter clinical testing
GeneDx RCV003719950 SCV005370736 uncertain significance not provided 2023-07-24 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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