ClinVar Miner

Submissions for variant NM_003283.6(TNNT1):c.792-114C>T

gnomAD frequency: 0.22262  dbSNP: rs891186
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000024553 SCV000971102 benign not provided 2018-06-18 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Leiden Muscular Dystrophy (TNNT1) RCV000024553 SCV000045857 not provided not provided 2012-03-18 no assertion provided curation

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