ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.-49CTCGGC[3]

dbSNP: rs769218713
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000187746 SCV000241343 benign not specified 2014-12-16 criteria provided, single submitter clinical testing The variant is found in EPILEPSY panel(s).

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