rs5030737(A;G)

Carrier of mannose binding deficiency but of low clinical importance

Magnitude
1.1Minor
Repute
Bad
Frequency
6%Average of 10 populations
On SNPedia
rs5030737(C;T)Minus strand
Gene
MBL2

Frequency

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

  • European ancestry (Utah)14%
  • Maasai (Kenya)11%
  • Tuscan10%
  • Gujarati Indian7%
  • Luhya (Kenya)4%
  • Mexican ancestry (Los Angeles)4%
  • Japanese (Tokyo)2%
  • African ancestry (Southwest US)2%
  • Han Chinese (Beijing)2%
  • Yoruba (Nigeria)<1%

Other genotypes of rs5030737

  1. G;GGoodcommon in clinvarTypical · 0.094% of people
  2. A;AMost notableBadmannose binding deficiency but of low clinical importanceMinor · 1.60% of people

All about rs5030737

Source and license

Adapted from rs5030737(C;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.