RS121912562 NR3C2

Health Risk Chr 4:148435252
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant pseudohypoaldosteronism type 1
Autism spectrum disorder
Autosomal dominant pseudohypoaldosteronism type 1
Autism spectrum disorder
Other Variants in NR3C2
rs2531829170 rs2531825719 rs1560949756 rs1560910156 rs121912563 rs1560735659 rs2531835861 rs121912564 rs121912565 rs121912566
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