rs6583817
A SNP in the IDE gene on chromosome 10. Its most notable genotype is C;T: ~0.80x (lower) risk for late onset Alzheimer's disease
- Gene
- IDE
- Location
- Chr 1092,487,490 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in complete genomics
- C;TMost notableGood~0.80x (lower) risk for late onset Alzheimer's disease
- T;TGood~0.80x (lower) risk for late onset Alzheimer's disease
On SNPedia: (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.
- AverageC;C 63% C;T 32% T;T 5%
- European ancestry (Utah)C;C 75% C;T 22% T;T 3%
- Han Chinese (Beijing)C;C 67% C;T 30% T;T 3%
- Japanese (Tokyo)C;C 56% C;T 34% T;T 11%
- Yoruba (Nigeria)C;C 43% C;T 48% T;T 10%
- African ancestry (Southwest US)C;C 35% C;T 58% T;T 7%
- Chinese (Denver)C;C 69% C;T 30% T;T <1%
- Gujarati IndianC;C 66% C;T 31% T;T 3%
- Luhya (Kenya)C;C 68% C;T 28% T;T 4%
- Mexican ancestry (Los Angeles)C;C 59% C;T 33% T;T 9%
- Maasai (Kenya)C;C 73% C;T 25% T;T 3%
- TuscanC;C 81% C;T 18% T;T 1%
Related
Conditions, medicines and genes
Other IDE SNPs
- rs7910977C;T~0.80x (lower) risk for late onset Alzheimer's diseaseMinor
- rs3758505A;Acommon in complete genomicsTypical
- rs3781239C;Ccommon in complete genomicsTypical
- rs4646954G;Gcommon in complete genomicsTypical
- rs4646958T;Tcommon in complete genomicsTypical
- rs7895832A;Acommon in complete genomicsTypical
- rs17107734C;Ccommon in complete genomicsTypical
Notes
From SNPedia
Show notes, about 220 words
rs6583817, also known as v311, is a SNP within an intron of the IDE gene, which encodes the insulin-degrading enzyme. Late onset Alzheimer's disease is a neurodegenerative condition in which the brain develops large numbers of extracellular senile plaques composed primarily of aggregated amyloid-B proteins as well as intraneuronal neurofibrillary tangles composed mainly of aggregated tau protein. One notable function of insulin-degrading enzyme is its ability to degrade amyloid-B and therefore to influence the amount of amyloid-B found in the brain. A study of ~3,000 patients (and an equal number of matched controls) found that carriers of one or two minor alleles, i.e. rs6583817(T), had ~2x higher levels of insulin-degrading enzyme (p < 10e-8), lower levels of amyloid-B, and a (slightly) lower risk of Alzheimer's disease, with an odds ratio of around 0.80 (p < 0.03), depending on the population studied. rs6583817 is thought to be a functional variant based on in vitro studies. While rs6583817 may be a functional variant, it is nearly perfectly linked to nearby SNP rs7910977, which is more commonly found on Illumina microarrays. The rs7910977(T) allele was also shown to correlate with decreased amyloid-B levels (presumably due to linkage with rs6583817), and it can be used to predict the presence of a rs6583817(T) allele.
Source and license
Adapted from rs6583817 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.