ClinVar Miner

Submissions for variant NM_015166.4(MLC1):c.526-118C>T

gnomAD frequency: 0.92233  dbSNP: rs4838882
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001527229 SCV001738177 benign Megalencephalic leukoencephalopathy with subcortical cysts 1 2021-06-10 criteria provided, single submitter clinical testing
GeneDx RCV001720299 SCV001947895 benign not provided 2018-11-12 criteria provided, single submitter clinical testing

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