ClinVar Miner

Submissions for variant NC_012920.1(MT-ND2):m.5095T>C

dbSNP: rs1556422950
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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 RCV000853863 SCV000996896 likely benign Leigh syndrome 2019-10-17 criteria provided, single submitter clinical testing The NC_012920.1:m.5095T>C (YP_003024027.1:p.Ile209Thr) variant in MTND2 gene is interpretated to be a Likely Benign variant based on the modified ACMG guidelines (unpublished). This variant meets the following evidence codes: BS1, BP6

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