ClinVar Miner

Submissions for variant m.10438A>G

dbSNP: rs121434456
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002247297 SCV002517721 pathogenic Mitochondrial disease 2022-05-04 criteria provided, single submitter clinical testing
OMIM RCV000010249 SCV000030473 pathogenic Mitochondrial encephalomyopathy 2004-08-01 no assertion criteria provided literature only

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