ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.2541+18G>A

dbSNP: rs12150090
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001713211 SCV001939541 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073343 SCV002404173 benign Koolen-de Vries syndrome 2025-02-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001713211 SCV005247059 benign not provided criteria provided, single submitter not provided

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