rs11545078
A SNP in the GGH gene on chromosome 8. Its most notable genotype is G;G: common on affy axiom data
- Gene
- GGH
- Location
- Chr 863,026,205 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 7%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs11545078 on the minus strand: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageG;G 82%
- European ancestry (Utah)G;G 78%
- Japanese (Tokyo)G;G 77%
- Yoruba (Nigeria)G;G 84%
- African ancestry (Southwest US)G;G 88%
- Chinese (Denver)G;G 87%
- Gujarati IndianG;G 72%
- Luhya (Kenya)G;G 86%
- Maasai (Kenya)G;G 85%
- TuscanG;G 84%
Related
Notes
From SNPedia
Notes
Epigenetic regulation of human gamma-glutamyl hydrolase activity in acute lymphoblastic leukemia cells.
Source and license
Adapted from rs11545078 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.