{{Rsnum
|rsid=104894161
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=EGR2
|position=62813563
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EGR2
}}{{omim
|id=129010
|rsnum=104894161
|variant=0004
}}{{ClinVar
|rsid=104894161
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=64573323
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=EGR2:1959
|GENE_NAME=EGR2
|GENE_ID=1959
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.64573323G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1205; 129010.0004
|CLNSIG=5
|CLNCUI=C1843247
|CLNDBN=Dejerine-sottas neuropathy, autosomal dominant; Charcot-Marie-Tooth disease, type ID; Dejerine-Sottas disease
|Disease=Dejerine-sottas neuropathy; Charcot-Marie-Tooth disease; Dejerine-Sottas disease
|CLNACC=RCV000018236.26; RCV000018237.22; RCV000032120.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1205:C1843247:607678:101084; NBK1205:NBK1468:C0011195:145900:64748:111499002
}}