rs7653
A SNP in the SAR1A gene on chromosome 10. Its most notable genotype is A;A: common/normal
- Gene
- SAR1A
- Location
- Chr 1070,150,560 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs7653 on the minus strand: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageA;A 97%
- European ancestry (Utah)A;A 91%
- Han Chinese (Beijing)A;A 100%
- Japanese (Tokyo)A;A 100%
- Yoruba (Nigeria)A;A 98%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 150 words
rs7653 represents a rare variant in the SAR1A gene on chromosome 10. A 2017 publication reports that the rs7653(C) allele may be associated with a lower odds of developing Alzheimer's disease in individuals otherwise at higher risk for the disorder. In ~400 individuals from the ADNI cohort tested, the rs7653(C) allele carriers had an odds ratio of 0.35 (p value = 0.0049) compared to non-carriers; however, in ~500 individuals from the CCS cohort subsequently tested, rs7653(C) carriers did not have a statistically significant difference from non-carriers, even though the authors reported that the association was in the "predicted positive direction". This is in contrast to the findings associated with rs142787485, which were significant in both cohorts. The 2017 publication describes the same research cited in a report from ICAD 2016 (page 4 and page 9 of this pdf.
Source and license
Adapted from rs7653 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.