{{Rsnum
|rsid=121908569
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=EIF2AK3
|position=88583430
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EIF2AK3
}}{{omim
|id=604032
|rsnum=121908569
|variant=0002
}}{{ClinVar
|rsid=121908569
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=88882948
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=EIF2AK3:9451
|GENE_NAME=EIF2AK3
|GENE_ID=9451
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.88882948C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604032.0002
|CLNSIG=5
|CLNCUI=C0432217
|CLNDBN=Wolcott-Rallison dysplasia
|Disease=Wolcott-Rallison dysplasia
|CLNACC=RCV000006233.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0432217:226980:1667:254066006
}}