ClinVar Miner

Submissions for variant NM_006073.4(TRDN):c.-26A>G

gnomAD frequency: 0.00045  dbSNP: rs372934247
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001707674 SCV000718502 likely benign not provided 2020-02-20 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003950260 SCV004761895 likely benign TRDN-related condition 2023-12-16 criteria provided, single submitter clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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