ClinVar Miner

Submissions for variant NM_004817.4(TJP2):c.-16G>T

gnomAD frequency: 0.00310  dbSNP: rs199557806
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252498 SCV000310662 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001582864 SCV001811786 likely benign not provided 2018-07-17 criteria provided, single submitter clinical testing

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