ClinVar Miner

Submissions for variant NM_012470.4(TNPO3):c.121-30T>G

gnomAD frequency: 0.00384  dbSNP: rs147557723
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001574526 SCV001801361 likely benign not provided 2018-08-14 criteria provided, single submitter clinical testing

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