rs3865418
A SNP in the NEDD4L gene on chromosome 18. Its most notable genotype is C;C: normal
- Gene
- NEDD4L
- Location
- Chr 1858,336,932 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 47%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableNot ratednormal
- C;TNot rated1.3x increased risk for hypertension
- G;GNot ratedNo summary available.
- T;TNot rated>1.3x increased risk for hypertension
On SNPedia: (C;C), (C;T), (G;G), (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 28% C;T 45% G;G 0% T;T 27%
- European ancestry (Utah)C;C 30% C;T 42% G;G 0% T;T 29%
- Han Chinese (Beijing)C;C 39% C;T 50% G;G 0% T;T 12%
- Japanese (Tokyo)C;C 50% C;T 43% G;G 0% T;T 7%
- Yoruba (Nigeria)C;C 14% C;T 44% G;G 0% T;T 42%
- African ancestry (Southwest US)C;C 25% C;T 46% G;G 0% T;T 30%
- Chinese (Denver)C;C 46% C;T 44% G;G 0% T;T 10%
- Gujarati IndianC;C 32% C;T 42% G;G 0% T;T 27%
- Luhya (Kenya)C;C 13% C;T 42% G;G 0% T;T 46%
- Mexican ancestry (Los Angeles)C;C 28% C;T 57% G;G 0% T;T 16%
- Maasai (Kenya)C;C 12% C;T 46% G;G 0% T;T 42%
- TuscanC;C 19% C;T 42% G;G 0% T;T 39%
Related
Notes
From SNPedia
Notes
rs3865418, a SNP in the NEDD4L gene, has been associated with hypertension in a study of Chinese (Hans) patients. Association under an additive model yielded an odds ratio of 1.31 (CI: 1.04-1.67, p=0.025) for the rs3865418(T) allele. The association remained significant (p = 0.039) after adjusting for age and sex, and was primarily associated with significantly higher diastolic blood pressure.
Source and license
Adapted from rs3865418 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.