ClinVar Miner

Submissions for variant NM_207346.3(TSEN54):c.521+39C>T

gnomAD frequency: 0.06538  dbSNP: rs57636645
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000147785 SCV000317254 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001689690 SCV001914237 benign not provided 2018-06-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001689690 SCV005251770 benign not provided criteria provided, single submitter not provided
Genetic Services Laboratory, University of Chicago RCV000147785 SCV000195256 likely benign not specified no assertion criteria provided clinical testing

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