ClinVar Miner

Submissions for variant NM_015166.4(MLC1):c.895-261A>G

gnomAD frequency: 0.09460  dbSNP: rs8136173
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001656874 SCV001865687 benign not provided 2021-06-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001656874 SCV005275846 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001827554 SCV002076177 benign Megalencephalic leukoencephalopathy with subcortical cysts 2019-09-09 no assertion criteria provided clinical testing

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