Gene entry
RARB
retinoic acid receptor beta
- Chromosome
- 3
- Cytoband
- 3p24.2
- Variants (rsID)
- 257
RARB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p24.2). Its official name is “retinoic acid receptor beta”. The reference table lists 257 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs397518483Pathogenicsingle nucleotide variantMicrophthalmia, syndromic 12|Inborn genetic diseases
Other listed variants
- rs188922
- rs321526
- rs322673
- rs322695
- rs322707
- rs1021701
- rs1021702
- rs1153589
- rs1286644
- rs1286733
- rs1286739
- rs1286762
- rs1286772
- rs1368266
- rs1384899
- rs1529672
- rs1529875
- rs1580813
- rs1580819
- rs1603974
- rs1603986
- rs1604003
- rs1656455
- rs1864903
- rs1864909
- rs1865614
- rs1909526
- rs1991784
- rs2033447
- rs2067964
- rs2362765
- rs2362771
- rs2362772
- rs2363517
- rs2363527
- rs2649616
- rs3773429
- rs3773439
- rs4081949
- rs4256093
- rs4280597
- rs4547662
- rs4568101
- rs4681027
- rs4681047
- rs4858142
- rs4858670
- rs4858694
- rs6550923
- rs6550928
- rs6550969
- rs6550971
- rs6550978
- rs6550979
- rs6763490
- rs6764521
- rs6765032
- rs6767543
- rs6769702
- rs6771747
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.