rs6195

A SNP in the NR3C1 gene on chromosome 5. Its most notable genotype is T;T.

Gene
NR3C1
Location
Chr 5143,399,752 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableNot ratedNo summary available.Typical · 0.00% of people

On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageT;T 0%
  • European ancestry (Utah)T;T 0%
  • Han Chinese (Beijing)T;T 0%
  • Gujarati IndianT;T 0%
  • Mexican ancestry (Los Angeles)T;T 0%

Notes

From SNPedia

Show notes, about 230 words

rs6195 (Asn363Ser/N363S) is a SNP within the NR3C1 (Nuclear receptor subfamily 3, group C, member 1 [glucocorticoid receptor]) gene. The common A allele encodes for Asparagine and the less common G allele encodes for Serine. Abstract linked to increased glucocorticoid sensitivity, coronary artery disease, and increased body mass index. Molecular evidence for a link between the N363S glucocorticoid receptor polymorphism and altered gene expression. Glucocorticoid receptor gene variant in the 3' untranslated region is associated with multiple measures of blood pressure. No association of glucocorticoid receptor polymorphisms with asthma and response to glucocorticoids. IL-10 and TNF-alpha promoter haplotypes are associated with childhood Crohn's disease location. Pharmacogenetic risk factors for altered bone mineral density and body composition in pediatric acute lymphoblastic leukemia. Glucocorticoid receptor gene polymorphisms do not affect growth in fetal and early postnatal life. The Generation R Study. Pharmacogenomic approaches to asthma treatment. Molecular mechanism of glucocorticoid resistance in inflammatory bowel disease. Genetic polymorphisms of the glucocorticoid receptor may affect the phenotype of women with anovulatory polycystic ovary syndrome. Glucocorticoid receptor polymorphism is associated with lithium response in bipolar patients.

Source and license

Adapted from rs6195 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.