rs11983798
A SNP in the ATXN7L1 gene on chromosome 7. Its most notable genotype is G;G: common genotype
- Gene
- ATXN7L1
- Location
- Chr 7105,640,741 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 6%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 7 HapMap populations.
- AverageG;G 90%
- European ancestry (Utah)G;G 97%
- Han Chinese (Beijing)G;G 96%
- Japanese (Tokyo)G;G 96%
- Yoruba (Nigeria)G;G 73%
- Chinese (Denver)G;G 98%
- Luhya (Kenya)G;G 84%
- TuscanG;G 89%
Notes
From SNPedia
Notes
Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. (PMID 22881374 PMCID:PMC3419486), see TABLE 4 for reference to rs11983798 T allele.
Source and license
Adapted from rs11983798 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.