{{Rsnum
|rsid=80358242
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MLC1
|position=50084727
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MLC1
}}{{omim
|id=605908
|rsnum=80358242
|variant=0009
}}{{ClinVar
|rsid=80358242
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50523156
|CHROM=22
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=MLC1:23209
|GENE_NAME=MLC1
|GENE_ID=23209
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.50523156C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1535; 605908.0009
|CLNSIG=5
|CLNCUI=C1858854; C1858854
|CLNDBN=Megalencephalic leukoencephalopathy with subcortical cysts 1
|Disease=Megalencephalic leukoencephalopathy with subcortical cysts 1
|CLNACC=RCV000004986.2
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1535:C1858854:604004:2478
}}{{PMID Auto
|PMID=12189496
|Title=Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews.
}}