{{Rsnum
|rsid = 29001571
|Gene=HSPB1
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=7
|position=76303816
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HSPB1
}}{{omim
|desc=NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB
|id=602195
|rsnum=29001571
|variant=0002
}}
{{ neighbor
| rsid = 28939680
| distance = 25
}}

{{ClinVar
|rsid=29001571
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=75933133
|CHROM=7
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=HSPB1:3315
|GENE_NAME=HSPB1
|GENE_ID=3315
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.75933133C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602195.0002
|CLNSIG=5
|CLNCUI=C2608087; C1847823
|CLNDBN=Distal hereditary motor neuronopathy type 2B; Charcot-Marie-Tooth disease type 2F
|Disease=Distal hereditary motor neuronopathy type 2B; Charcot-Marie-Tooth disease type 2F
|CLNACC=RCV000007906.1; RCV000007907.2
|Tags=PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C2608087:608634:139525; NBK1285:C1847823:606595:99940
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | Illumina Human 1M}}