rs5522
A SNP in the NR3C2 gene on chromosome 4. Its most notable genotype is T;T: common on affy axiom data
- Gene
- NR3C2
- Location
- Chr 4148,436,323 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 12%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableGoodcommon on affy axiom data
- C;CGoodcommon in clinvar
- A;ANot ratedNo summary available.
SNPedia records rs5522 on the minus strand: (A;A), (G;G), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageT;T 79% C;C 2% A;A 0%
- European ancestry (Utah)T;T 81% C;C <1% A;A 0%
- Han Chinese (Beijing)T;T 73% C;C 3% A;A 0%
- Japanese (Tokyo)T;T 64% C;C 7% A;A 0%
- Yoruba (Nigeria)T;T 83% C;C <1% A;A 0%
- African ancestry (Southwest US)T;T 93% C;C 2% A;A 0%
- Chinese (Denver)T;T 77% C;C 2% A;A 0%
- Gujarati IndianT;T 86% C;C 0% A;A 0%
- Luhya (Kenya)T;T 82% C;C 0% A;A 0%
- Mexican ancestry (Los Angeles)T;T 71% C;C 2% A;A 0%
- Maasai (Kenya)T;T 72% C;C 1% A;A 0%
- TuscanT;T 86% C;C 0% A;A 0%
Related
Source and license
Adapted from rs5522 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.