ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.-89-17T>C

gnomAD frequency: 0.00001  dbSNP: rs1051577933
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000442672 SCV000524054 likely benign not specified 2016-02-15 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.
Fulgent Genetics, Fulgent Genetics RCV002502533 SCV002806433 likely benign Koolen-de Vries syndrome 2021-12-14 criteria provided, single submitter clinical testing

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