{{Rsnum
|rsid=397514647
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=EIF2B3
|position=44981089
|Gene_s=EIF2B3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000033201.1
|CLNALLE=1
|CLNDBN=Leukoencephalopathy with vanishing white matter
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1258:C1858991:603896:ORPHA135
|CLNHGVS=NC_000001.11:g.44981089A>T
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_020365.4:c.80T>A; 606273.0005
|Disease=Leukoencephalopathy with vanishing white matter
|FwdALT=A
|FwdREF=T
|GENEINFO=EIF2B3:8891
|GENE_ID=8891
|GENE_NAME=EIF2B3
|REF=A
|RSPOS=44981089
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=136
|rsid=397514647
|CLNORIGIN=1
}}