{{Rsnum
|rsid = 28939680
|Gene=HSPB1
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=7
|position=76303841
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HSPB1
}}{{omim
|desc=CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
|id=602195
|rsnum=28939680
|variant=0001
}}
{{ neighbor
| rsid = 28939681
| distance = 2
}}

{{ neighbor
| rsid = 29001571
| distance = 25
}}

{{ClinVar
|rsid=28939680
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=75933158
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HSPB1:3315
|GENE_NAME=HSPB1
|GENE_ID=3315
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.75933158C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602195.0001
|CLNSIG=5
|CLNCUI=C1847823; C2608087
|CLNDBN=Charcot-Marie-Tooth disease type 2F; Distal hereditary motor neuronopathy type 2B
|Disease=Charcot-Marie-Tooth disease type 2F; Distal hereditary motor neuronopathy type 2B
|CLNACC=RCV000007904.2; RCV000007905.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1285:C1847823:606595:99940; C2608087:608634:139525
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}