{{Rsnum
|rsid=113994014
|Chromosome=14
|Orientation=plus
|geno1=(ATGGCT;ATGGCT)
|geno2=(ATGGCT;TG)
|geno3=(TG;TG)
|Gene=EIF2B2
|position=75005875
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EIF2B2
}}{{omim
|id=606454
|rsnum=113994014
|variant=0005
}}{{ClinVar
|rsid=113994014
|Reversed=0
|FwdREF=ATGGCT
|FwdALT=TG
|REF=AATGGCT
|ALT=ATG
|RSPOS=75472577
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=EIF2B2:8892
|GENE_NAME=EIF2B2
|GENE_ID=8892
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.75472578_75472583delATGGCTinsTG
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000004588.1
|CLNDBN=Ovarioleukodystrophy
|CLNDSDB=MedGen
|CLNDSDBID=C1847967
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606454.0005
|Disease=Ovarioleukodystrophy
}}{{PMID|12707859|OA=1
}} Ovarian failure related to eukaryotic initiation factor 2B mutations.

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