rs33971440

A SNP in the HBB gene on chromosome 11. Its most notable genotype is T;T: Beta Thalassemia major; Hemoglobin beta-zero; possibly transfusion dependent

Gene
HBB
Location
Chr 115,226,929 (GRCh38)
Highest magnitude
5.5Very important
Tested on
23andMe
Minor allele frequency
<1%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

SNPedia records rs33971440 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

T;T

see HBB

C;T

see discussion at HBB

Source and license

Adapted from rs33971440 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.