ClinVar Miner

Submissions for variant NM_015166.4(MLC1):c.-59-17T>C

gnomAD frequency: 0.03393  dbSNP: rs9628323
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 RCV001643357 SCV001857907 benign not provided 2021-05-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001643357 SCV005275870 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001832833 SCV002081612 benign Megalencephalic leukoencephalopathy with subcortical cysts 2019-10-17 no assertion criteria provided clinical testing

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