rs3818361
A SNP in the CR1 gene on chromosome 1. Its most notable genotype is A;A: 1.2x increased risk for late-onset Alzheimer's
- Gene
- CR1
- Location
- Chr 1207,611,623 (GRCh38)
- Highest magnitude
- 1.2Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 27%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GNot ratednormal
- A;GBad1.15x increased risk for late-onset Alzheimer's
- A;AMost notableBad1.2x increased risk for late-onset Alzheimer's
SNPedia records rs3818361 on the minus strand: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageG;G 50% A;G 40% A;A 10%
- European ancestry (Utah)G;G 58% A;G 32% A;A 10%
- Han Chinese (Beijing)G;G 42% A;G 45% A;A 12%
- Japanese (Tokyo)G;G 50% A;G 38% A;A 12%
- Yoruba (Nigeria)G;G 30% A;G 48% A;A 22%
- African ancestry (Southwest US)G;G 28% A;G 54% A;A 18%
- Chinese (Denver)G;G 44% A;G 42% A;A 14%
- Gujarati IndianG;G 89% A;G 10% A;A 1%
- Luhya (Kenya)G;G 32% A;G 62% A;A 6%
- Mexican ancestry (Los Angeles)G;G 76% A;G 24% A;A 0%
- Maasai (Kenya)G;G 37% A;G 48% A;A 15%
- TuscanG;G 63% A;G 33% A;A 4%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs3818361 is a SNP associated with the complement component (3b/4b) receptor 1 CR1 gene. The association of this SNP and late-onset Alzheimer's disease was replicated over a total of another 1829 cases (and 2576 controls). The odds ratio for rs3818361(T) allele was 1.15 (note the p value was 0.014).
Source and license
Adapted from rs3818361 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.