ClinVar Miner

Submissions for variant NM_001365902.3(NFIX):c.1402+85C>T

gnomAD frequency: 0.00674  dbSNP: rs182674881
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001589799 SCV001815264 likely benign not provided 2018-10-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001589799 SCV005209514 likely benign not provided criteria provided, single submitter not provided

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