ClinVar Miner

Submissions for variant NC_000008.11:g.124557903G>A

gnomAD frequency: 0.71134  dbSNP: rs4870903
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
Mendelics RCV000988114 SCV001137705 benign Mitochondrial complex 1 deficiency, nuclear type 24 2019-05-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004712952 SCV005270790 benign not provided criteria provided, single submitter not provided

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