rs3781239
A SNP in the IDE gene on chromosome 10. Its most notable genotype is C;C: common in complete genomics
- Gene
- IDE
- Location
- Chr 1092,458,040 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 3%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3781239 on the minus strand: (G;G). 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.
- AverageC;C 94%
- European ancestry (Utah)C;C 100%
- Han Chinese (Beijing)C;C 80%
- Japanese (Tokyo)C;C 96%
- Yoruba (Nigeria)C;C 100%
Related
Other IDE SNPs
- rs6583817C;T~0.80x (lower) risk for late onset Alzheimer's diseaseMinor
- rs7910977C;T~0.80x (lower) risk for late onset Alzheimer's diseaseMinor
- rs3758505A;Acommon in complete genomicsTypical
- rs4646954G;Gcommon in complete genomicsTypical
- rs4646958T;Tcommon in complete genomicsTypical
- rs7895832A;Acommon in complete genomicsTypical
- rs17107734C;Ccommon in complete genomicsTypical
Source and license
Adapted from rs3781239 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.