RS368322580 NR3C2

Health Risk Chr 4:148154829
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant pseudohypoaldosteronism type 1
Inborn genetic diseases
Pseudohyperaldosteronism type 2
Autosomal dominant pseudohypoaldosteronism type 1
Inborn genetic diseases
Pseudohyperaldosteronism type 2
Other Variants in NR3C2
rs2531829170 rs2531825719 rs121912562 rs1560949756 rs1560910156 rs121912563 rs1560735659 rs2531835861 rs121912564 rs121912565
Ask Dr. Hemsworth about this variant