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Gene entry

CX3CR1

C-X3-C motif chemokine receptor 1

Chromosome
3
Cytoband
3p22.2
Variants (rsID)
7

CX3CR1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p22.2). Its official name is “C-X3-C motif chemokine receptor 1”. The reference table lists 7 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs3732378Othersingle nucleotide variantDevelopmental Dysplasia of the Hip 1|Macular Degeneration, Age-Related, 1|End Stage Renal Disease|Oligohydramnios|Eye Disease|Vascular Disease|Atrial Standstill 1|Dilated Cardiomyopathy|Alzheimer Disease|Atherosclerosis Susceptibility|Lateral Sclerosis|Human Immunodeficiency Virus Type 1|Amyotrophic Lateral Sclerosis 1|Macular Degeneration, Age-Related, 12|Developmental Dysplasia of the Hip 2|Cerebrovascular Disease
  • rs3732379Othersingle nucleotide variantMacular Degeneration, Age-Related, 12|Macular Degeneration, Age-Related, 1|Eye Disease|Developmental Dysplasia of the Hip 1|End Stage Renal Disease|Atrial Standstill 1|Dilated Cardiomyopathy|Alzheimer Disease|Atherosclerosis Susceptibility|Lateral Sclerosis|Amyotrophic Lateral Sclerosis 1|Arteriosclerosis|Cerebrovascular Disease

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.