rs33950507

A SNP in the HBB gene on chromosome 11. Its most notable genotype is T;T: reduction in malarial risk; mild anemia

Gene
HBB
Location
Chr 115,226,943 (GRCh38)
Highest magnitude
4.5Very important
Tested on
23andMe, AncestryDNA
Minor allele frequency
<1%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableBadreduction in malarial risk; mild anemiaVery important · 4.5
  2. C;TNot ratedreduction in malarial risk; carrier of beta thalassemia mutationImportant · 3.0
  3. C;CGoodnormalTypical · 0.0

SNPedia records rs33950507 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Notes

From SNPedia

Notes

rs33950507 is a SNP found in the beta hemoglobin HBB gene, not far from the well-known SNP associated with malarial resistance (rs334, Hb S). This SNP gives rise to the "Hb E", or hemoglobin E, form of hemoglobin as the HBB forms are commonly named. It is found primarily in Southeast Asia. rs33950507(A) is associated with somewhat increased malarial resistance, and in homozygous (A;A) state, with mild hypochromic microcytic anemia. Microarray-based estimation of SNP allele-frequency in pooled DNA using the Langmuir kinetic model.

T;T

see HBB

C;T

see HBB

Source and license

Adapted from rs33950507 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.