ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.-90+24CCT[3]

dbSNP: rs143625699
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000289114 SCV000403670 benign Syndromic intellectual disability 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001618567 SCV001845130 benign not provided 2018-06-23 criteria provided, single submitter clinical testing

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