ClinVar Miner

Submissions for variant NM_004553.6(NDUFS6):c.132+26A>C

gnomAD frequency: 0.85626  dbSNP: rs2242412
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001543890 SCV001762782 benign Mitochondrial complex 1 deficiency, nuclear type 9 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001713002 SCV001940766 benign not provided 2018-06-23 criteria provided, single submitter clinical testing

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