{{Rsnum
|rsid=104894345
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HSPB8
|position=119187080
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HSPB8
}}{{omim
|id=608014
|rsnum=104894345
|variant=0001
}}{{ClinVar
|rsid=104894345
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=119624885
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050260000000000002110100
|GENEINFO=HSPB8:26353
|GENE_NAME=HSPB8
|GENE_ID=26353
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000012.11:g.119624885G>C; NC_000012.11:g.119624885G>T
|CLNSRCID=
608014.0001; 608014.0003
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000002735.1; RCV000002737.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDBN=Distal hereditary motor neuronopathy type 2A; Charcot-Marie-Tooth disease, type 2L
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1834692:158590:139525; NBK1285:C1837552:608673:99945
|CLNSRC=OMIM Allelic Variant
|Disease=Distal hereditary motor neuronopathy type 2A; Charcot-Marie-Tooth disease
}}