{{Rsnum
|rsid=387906347
|Chromosome=9
|position=36219856
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GNE
|Gene_s=GNE
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=9
|CLNACC=RCV000006398.1
|CLNALLE=1
|CLNDBN=Inclusion body myopathy 2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1262:C1833373:600737:602
|CLNHGVS=NC_000009.11:g.36219853C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603824.0007
|Disease=Inclusion body myopathy 2
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=36219853
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a01000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387906347
}}