rs3819299(G;G)

Likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes.

Magnitude
3.0Important
Repute
Bad
Frequency
0%Average of 11 populations
On SNPedia
rs3819299(C;C)Minus strand
Gene
HLA-B

Frequency

Share of people with G;G in each HapMap population.

  • European ancestry (Utah)0%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%
  • African ancestry (Southwest US)0%
  • Chinese (Denver)0%
  • Gujarati Indian0%
  • Luhya (Kenya)0%
  • Mexican ancestry (Los Angeles)0%
  • Maasai (Kenya)0%
  • Tuscan0%

Other genotypes of rs3819299

  1. T;TGoodcommon in clinvarTypical · 0.089% of people
  2. G;TMost notableBadlikely to carry one HLA-B27 allele, possible risk for B27 Syndromes.Important · 3.011% of people

All about rs3819299

Notes

From SNPedia

See details at: HLA-B27 Syndromes. Not all allelles of HLA-B27 are at risk for B27 Syndromes, please check the HLA-B27 page for details.

Source and license

Adapted from rs3819299(C;C) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.