ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.2874G>A (p.Gln958=)

dbSNP: rs1010687863
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002169438 SCV002335792 likely benign Koolen-de Vries syndrome 2021-03-07 criteria provided, single submitter clinical testing

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