ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.*1328del

dbSNP: rs71665335
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000368058 SCV000403580 benign Syndromic intellectual disability 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000352483 SCV000483631 benign MAPT-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing

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