rs10868025
A SNP in the FRMD3 gene on chromosome 9. Its most notable genotype is G;G.
- Gene
- FRMD3
- Location
- Chr 983,549,261 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 30%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). 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 9%
- European ancestry (Utah)G;G 11%
- Han Chinese (Beijing)G;G 15%
- Japanese (Tokyo)G;G 8%
- Yoruba (Nigeria)G;G 0%
- African ancestry (Southwest US)G;G 2%
- Chinese (Denver)G;G 15%
- Gujarati IndianG;G 7%
- Luhya (Kenya)G;G <1%
- Mexican ancestry (Los Angeles)G;G 19%
- Maasai (Kenya)G;G 3%
- TuscanG;G 16%
Notes
From SNPedia
Show notes, about 350 words
rs10868025 is associated with diabetic nephropathy, a kidney disease resulting from poorly managed diabetes and genetic factors. When a person has diabetic nephropathy, excess levels of blood sugar cause damage to blood vessels within the nephrons, which are filtering units within the kidneys. Diabetic nephropathy is the number one cause of long-term kidney failure and end-stage kidney disease in the United States ncbi.nlm.nih.gov. Some of the first evidence for a genetic factor in the development of this disease was published in a New England Journal of Medicine paper in 1989 . However, causal variants have yet to be identified . This could potentially be due to different variants being responsible for different stages of the disease . In a study, researchers found an association between rs10868025 (9q85.4) and diabetic nephropathy . In this study, genome wide scans were first performed on the GoKinD collection with 885 case and 820 control subjects on an Affymetrix array, and putative markers were then screened in a follow-up study looking for association between these markers and time-to-onset of nephropathy in the DCCT/EDIC data, which contained 132 cases of nephropathy and used an Illumina array. In the former analysis, the odds ratio for rs10868025 was 1.45, with a 95% confidence interval of (1.25-1.67) and a p-value of 5e-7, though this was not low enough to achieve genome-wide significance in the study (needed 1.4e-7). G is the non-risk allele and A is the risk allele. In the latter analysis, rs13289150 (r^2 = 1.0 with rs10868025) was used instead of rs10868025 and found to be significantly associated with time-to-onset of nephropathy (p-value = 0.05). While rs10868025 is not in a gene, it is located near the FRMD3 gene, which is part of the 4.1 protein ezrin, radixin, moesin (FERM) domain. It was found in this study that cell lines relevant to diabetic nephropathy express this gene. FRMD3 encodes the 4.1O protein, which contains a FERM domain that is necessary for maintaining the integrety of the cellular membrane.
Source and license
Adapted from rs10868025 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.