{{Rsnum
|rsid=113994006
|Gene=EIF2B1
|Chromosome=12
|position=123630396
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=EIF2B1
}}{{omim
|id=606686
|rsnum=113994006
|variant=0001
}}{{ClinVar
|rsid=113994006
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=124114943
|CHROM=12
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000016110100
|GENEINFO=EIF2B1:1967
|GENE_NAME=EIF2B1
|GENE_ID=1967
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.124114943C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=606686.0001
|CLNSIG=5
|CLNCUI=C1858991
|CLNDBN=Leukoencephalopathy with vanishing white matter
|Disease=Leukoencephalopathy with vanishing white matter
|CLNACC=RCV000004339.1
|Tags=RV;PM;PMC;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1258:C1858991:603896:135
|COMMON=0
}}{{PMID Auto
|PMID=11835386
|Title=Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter.
}}

{{PMID Auto
|PMID=14572143
|Title=Leukoencephalopathy with vanishing white matter: from magnetic resonance imaging pattern to five genes.
}}