{{Rsnum
|rsid=104894160
|Chromosome=10
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=EGR2
|position=62813491
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EGR2
}}{{omim
|id=129010
|rsnum=104894160
|variant=0003
}}{{ClinVar
|rsid=104894160
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=64573251
|CHROM=10
|dbSNPBuildID=137
|SSR=0
|SAO=0
|VP=0x050360000000000002110100
|GENEINFO=EGR2:1959
|GENE_NAME=EGR2
|GENE_ID=1959
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.64573251C>A
|CLNSIG=5
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000018235.26; RCV000032122.1
|CLNDBN=Neuropathy, congenital hypomyelinating, autosomal dominant; Congenital hypomyelinating neuropathy
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1205:NBK1468:C0393818:605253:99951:230562000
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1205; 129010.0003
|Disease=Neuropathy; Congenital hypomyelinating neuropathy
}}