{{Rsnum
|rsid=397514648
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=EIF2B2
|position=75003365
|Gene_s=EIF2B2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=14
|CLNACC=RCV000033202.1
|CLNALLE=1
|CLNDBN=Leukoencephalopathy with vanishing white matter
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1258:C1858991:603896:135
|CLNHGVS=NC_000014.8:g.75470068T>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606454.0006
|Disease=Leukoencephalopathy with vanishing white matter
|FwdALT=A
|FwdREF=T
|GENEINFO=EIF2B2:8892
|GENE_ID=8892
|GENE_NAME=EIF2B2
|REF=T
|RSPOS=75470068
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514648
}}