ClinVar Miner

Submissions for variant NC_012920.1(MT-TD):m.7582C>T

dbSNP: rs1603221026
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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 RCV000850933 SCV000993167 uncertain significance MELAS syndrome 2019-07-12 criteria provided, single submitter clinical testing The NC_012920.1:m.7582C>T variant in MT-TD gene is interpreted to be a Unknown Significance variant based on the modified ACMG guidelines (unpublished). This variant meets the following evidence codes reported in the guidelines: PM10, PP3, PP6, PP7

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