{{Rsnum
|rsid=121908625
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GNE
|position=36219927
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GNE
}}{{omim
|id=603824
|rsnum=121908625
|variant=0006
}}{{ClinVar
|rsid=121908625
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=36219924
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GNE:10020
|GENE_NAME=GNE
|GENE_ID=10020
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.36219924C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603824.0006
|CLNSIG=5
|CLNCUI=C1833373
|CLNDBN=Inclusion body myopathy 2
|Disease=Inclusion body myopathy 2
|CLNACC=RCV000006397.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1262:C1833373:600737:602
}}