ClinVar Miner

Submissions for variant NC_012920.1(MT-ND2):m.5186A>T

dbSNP: rs878939965
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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 RCV000853869 SCV000996902 benign Leigh syndrome 2019-10-17 criteria provided, single submitter clinical testing The NC_012920.1:m.5186A>T (YP_003024027.1:p.Trp239Cys) variant in MTND2 gene is interpretated to be a Benign variant based on the modified ACMG guidelines (unpublished).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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