rs13202464(A;G)

Likely to be a carrier of one HLA-B27 allele, possible risk for B27 Syndromes.

Magnitude
3.0Important
Repute
Bad
Frequency
12%Average of 11 populations
On SNPedia
rs13202464(A;G)
Gene
FGFR3P1

Frequency

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

  • Japanese (Tokyo)29%
  • Gujarati Indian27%
  • Han Chinese (Beijing)18%
  • Mexican ancestry (Los Angeles)14%
  • Chinese (Denver)13%
  • European ancestry (Utah)11%
  • African ancestry (Southwest US)7%
  • Maasai (Kenya)6%
  • Tuscan5%
  • Luhya (Kenya)<1%
  • Yoruba (Nigeria)0%

Other genotypes of rs13202464

  1. A;AGoodcommon/normalTypical · 0.088% of people
  2. G;GBadlikely to carry two HLA-B27 alleles, possible risk for B27 Syndromes.Important · 3.0<1% of people

All about rs13202464

Notes

From SNPedia

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

Source and license

Adapted from rs13202464(A;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.