ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.723A>G (p.Ala241=)

gnomAD frequency: 0.00001  dbSNP: rs375054119
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000601673 SCV000719011 likely benign not specified 2017-05-03 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV001469441 SCV001673521 likely benign Koolen-de Vries syndrome 2019-07-05 criteria provided, single submitter clinical testing

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