ClinVar Miner

Submissions for variant NM_024407.5(NDUFS7):c.544+140C>T

gnomAD frequency: 0.05844  dbSNP: rs73515052
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001683892 SCV001897789 benign not provided 2018-06-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001683892 SCV005308846 benign not provided criteria provided, single submitter not provided

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