ClinVar Miner

Submissions for variant NM_144736.5(NDUFAF7):c.408+45T>G

gnomAD frequency: 0.02216  dbSNP: rs115423532
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001776561 SCV002013215 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001776561 SCV005263374 likely benign not provided criteria provided, single submitter not provided

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