rs6189
A SNP in the NR3C1 gene on chromosome 5. Its most notable genotype is C;C: common in complete genomics
- Gene
- NR3C1
- Location
- Chr 5143,400,774 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 1%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs6189 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in one HapMap population.
- Maasai (Kenya)C;C 97%
Related
Other NR3C1 SNPs
- rs6190C;Ccommon in complete genomicsTypical
- rs6193T;Tcommon in clinvarTypical
- rs6195T;TNo summary available.Typical
- rs6196A;Acommon in complete genomicsTypical
- rs6198T;Tcommon in clinvarTypical
- rs2918419T;Tcommon in complete genomicsTypical
- rs9324921C;Ccommon genotypeTypical
- rs56149945T;Tcommon in clinvarTypical
Source and license
Adapted from rs6189 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.