ClinVar Miner

Submissions for variant NM_015965.7(NDUFA13):c.94+1G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003458945 SCV004183499 likely pathogenic Mitochondrial complex 1 deficiency, nuclear type 28 2023-10-16 criteria provided, single submitter clinical testing
Baylor Genetics RCV003455844 SCV004183539 likely pathogenic Hurthle cell carcinoma of thyroid 2023-10-16 criteria provided, single submitter clinical testing

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