ClinVar Miner

Submissions for variant NM_015166.4(MLC1):c.177+15A>G

gnomAD frequency: 0.00092  dbSNP: rs148099137
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665035 SCV000789091 likely benign Megalencephalic leukoencephalopathy with subcortical cysts 1 2017-01-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060809 SCV002460934 benign not provided 2024-01-25 criteria provided, single submitter clinical testing

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