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Gene entry

CYP7B1

cytochrome P450 family 7 subfamily B member 1

Chromosome
8
Cytoband
8q12.3
Variants (rsID)
58

CYP7B1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q12.3). Its official name is “cytochrome P450 family 7 subfamily B member 1”. The reference table lists 58 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs59035258Benignsingle nucleotide variantHereditary spastic paraplegia 5A|Spastic paraplegia|Hereditary spastic paraplegia
  • rs118000312Conflicting interpretationssingle nucleotide variantHereditary spastic paraplegia 5A|Hereditary spastic paraplegia
  • rs377119798Conflicting interpretationssingle nucleotide variantSpastic paraplegia|Hereditary spastic paraplegia 5A
  • rs116171274Pathogenicsingle nucleotide variantHereditary spastic paraplegia 5A|Spastic paraplegia|Hereditary spastic paraplegia
  • rs121908611Pathogenicsingle nucleotide variantHereditary spastic paraplegia 5A|Spastic paraplegia|Hereditary spastic paraplegia
  • rs121908613Pathogenicsingle nucleotide variantHereditary spastic paraplegia 5A|Hereditary spastic paraplegia|Spastic paraplegia

Other listed variants

Public references

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