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Gene entry

CD36

CD36 molecule (CD36 blood group)

Chromosome
7
Cytoband
7q21.11
Variants (rsID)
32

CD36 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q21.11). Its official name is “CD36 molecule (CD36 blood group)”. The reference table lists 32 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs3173798Benignsingle nucleotide variantPlatelet-type bleeding disorder 10
  • rs3211893Benignsingle nucleotide variantPlatelet-type bleeding disorder 10|Coronary heart disease, susceptibility to, 7|Malaria, susceptibility to|Platelet-type bleeding disorder 10
  • rs3211938Conflicting interpretationssingle nucleotide variantPlatelet-type bleeding disorder 10|Malaria, cerebral, susceptibility to
  • rs75326924Pathogenicsingle nucleotide variantPlatelet-type bleeding disorder 10|Inherited bleeding disorder, platelet-type
  • rs200067322Uncertain significancesingle nucleotide variantPlatelet-type bleeding disorder 10

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.