ClinVar Miner

Submissions for variant NC_012920.1:m.9478T>C

dbSNP: rs587776437
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 RCV002247533 SCV002518292 uncertain significance not specified 2022-05-04 criteria provided, single submitter clinical testing
GeneReviews RCV000144007 SCV000188899 not provided Leigh syndrome no assertion provided literature only

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