Gene entry
NR3C2
nuclear receptor subfamily 3 group C member 2
- Chromosome
- 4
- Cytoband
- 4q31.23
- Variants (rsID)
- 77
NR3C2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q31.23). Its official name is “nuclear receptor subfamily 3 group C member 2”. The reference table lists 77 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs2070951Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1
- rs2871Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1
- rs5522Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1
- rs5525Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1
- rs61759976Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1
Other listed variants
- rs1403143
- rs1490453
- rs1512343
- rs1879827
- rs2070950
- rs2883929
- rs3846317
- rs3846322
- rs3846328
- rs3846329
- rs3910054
- rs3931397
- rs4635799
- rs4835490
- rs6535594
- rs6810951
- rs6812904
- rs6817925
- rs6836191
- rs6844155
- rs6857011
- rs6858581
- rs7658048
- rs7698307
- rs10012553
- rs10519963
- rs11736161
- rs11737660
- rs12641471
- rs13116332
- rs17024387
- rs17024506
- rs17024706
- rs17024708
- rs17484454
- rs17581898
- rs17620330
- rs28594566
- rs34372017
- rs34438391
- rs34927488
- rs35337326
- rs55969126
- rs61757488
- rs61757901
- rs61758261
- rs61760027
- rs61762827
- rs61762855
- rs61764254
- rs62333652
- rs72655204
- rs72726656
- rs72726692
- rs72729966
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.