rs11978267(G;G)
Possible increased risk for infant acute myeloid leukemia (AML)
- Magnitude
- 2.0Worth knowing
- Repute
- Bad
- Frequency
- 5%Average of 11 populations
- On SNPedia
- rs11978267(G;G)
- Gene
- IKZF1
Frequency
Share of people with G;G in each HapMap population.
- Gujarati Indian16%
- European ancestry (Utah)7%
- Tuscan7%
- Yoruba (Nigeria)7%
- Luhya (Kenya)6%
- African ancestry (Southwest US)5%
- Chinese (Denver)4%
- Maasai (Kenya)3%
- Han Chinese (Beijing)3%
- Japanese (Tokyo)<1%
- Mexican ancestry (Los Angeles)0%
Other genotypes of rs11978267
Notes
From SNPedia
Although based on a fairly small study (~170 pediatric patients), homozygosity for this relatively rare IKZF1 gene allele has been reported to increase risk (perhaps 3+ fold) of infant acute myeloid leukemia (AML).
Source and license
Adapted from rs11978267(G;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.