ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.2298A>G (p.Pro766=)

gnomAD frequency: 0.00004  dbSNP: rs367624499
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000558326 SCV000645045 likely benign Koolen-de Vries syndrome 2021-05-21 criteria provided, single submitter clinical testing
GeneDx RCV001618729 SCV001846900 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing

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