ClinVar Miner

List of variants in gene combination HEPACAM, HEPN1 reported as likely benign for leukoencephalopathy, megalencephalic

Included ClinVar conditions (8):

Megalencephalic leukoencephalopathy with subcortical cysts
Megalencephalic leukoencephalopathy with subcortical cysts 1
Megalencephalic leukoencephalopathy with subcortical cysts 1; Megalencephalic leukoencephalopathy with subcortical cysts 2A; Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability
Megalencephalic leukoencephalopathy with subcortical cysts 2A
Megalencephalic leukoencephalopathy with subcortical cysts 2A; Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability
Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability
Megalencephalic leukoencephalopathy with subcortical cysts 3
Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_152722.5(HEPACAM):c.*472T>G	rs372662415	0.00133
NM_152722.5(HEPACAM):c.*1479T>C	rs566864287
NM_152722.5(HEPACAM):c.*831G>T	rs115556036

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