{{Rsnum
|rsid=139425890
|Gene=GNE
|Chromosome=9
|position=36246120
|Orientation=plus
|GMAF=0.0009183
|Gene_s=GNE
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=A
|CAF=0.9991; 0.0009183
|CHROM=9
|CLNACC=RCV000034132.2
|CLNALLE=1
|CLNDBN=Inclusion body myopathy 2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1262:C1833373:600737:602
|CLNHGVS=NC_000009.11:g.36246117T>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1262
|COMMON=1
|Disease=Inclusion body myopathy 2
|FwdALT=A
|FwdREF=T
|GENEINFO=GNE:10020
|GENE_ID=10020
|GENE_NAME=GNE
|REF=T
|RSPOS=36246117
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000416110100
|WGT=0
|dbSNPBuildID=134
|rsid=139425890
}}