ClinVar Miner

Submissions for variant NC_012920.1(MT-ATP6):m.8588T>C

dbSNP: rs1603221606
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine RCV000854249 SCV000997282 benign Leigh syndrome 2019-10-17 criteria provided, single submitter clinical testing The NC_012920.1:m.8588T>C (YP_003024031.1:p.Val21Ala) variant in MTATP6 gene is interpretated to be a Benign variant based on the modified ACMG guidelines (unpublished). This variant meets the following evidence codes: BS1, BS4

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