Gene entry

HSPB8

heat shock protein family B (small) member 8

Chromosome: 12
Cytoband: 12q24.23
Variants (rsID): 8

HSPB8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q24.23). Its official name is “heat shock protein family B (small) member 8”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs148514935Benignsingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2L|Neuronopathy, distal hereditary motor, type 2A

Other listed variants

rs11064694
rs11064703
rs73213453
rs75966754
rs78852656
rs117226603
rs144888613

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.