rs4273077(A;A)

Normal risk for development of MGUS

Magnitude
1.0Minor
Repute
Good
Frequency
61%Average of 11 populations
On SNPedia
rs4273077(A;A)
Gene
TNFRSF13B

Frequency

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

  • Luhya (Kenya)79%
  • European ancestry (Utah)79%
  • Tuscan78%
  • Maasai (Kenya)78%
  • African ancestry (Southwest US)77%
  • Yoruba (Nigeria)69%
  • Mexican ancestry (Los Angeles)67%
  • Gujarati Indian66%
  • Han Chinese (Beijing)31%
  • Japanese (Tokyo)28%
  • Chinese (Denver)22%

Other genotypes of rs4273077

  1. A;GBadPossibly slight 1.09x risk for development of MGUSMinor · 1.032% of people
  2. G;GMost notableBad3.57x increased risk of MGUSWorth knowing · 2.07% of people

All about rs4273077

Notes

From SNPedia

This was defined as an OR of 1.0 for the development of MGUS (Monoclonal Gammopathy of Uncertain Significance). A is the major allele and not the risk allele.

Source and license

Adapted from rs4273077(A;A) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.