rs11746443

A SNP in the RGS14 gene on chromosome 5. Its most notable genotype is A;A: 1.19x risk of kidney stone in Japanese

Gene
RGS14
Location
Chr 5177,371,305 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
19%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableBad1.19x risk of kidney stone in JapaneseTypical · 0.04% of people
  2. A;GBad1.19x risk of kidney stone in JapaneseTypical · 0.025% of people
  3. G;GGoodnormalTypical · 0.071% of people

On SNPedia: (A;A), (A;G), (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.

  • AverageA;A 4% A;G 25% G;G 71%
  • European ancestry (Utah)A;A 11% A;G 38% G;G 51%
  • Han Chinese (Beijing)A;A 4% A;G 29% G;G 68%
  • Japanese (Tokyo)A;A 3% A;G 34% G;G 64%
  • Yoruba (Nigeria)A;A <1% A;G 10% G;G 90%
  • African ancestry (Southwest US)A;A 2% A;G 16% G;G 83%
  • Chinese (Denver)A;A 3% A;G 23% G;G 74%
  • Gujarati IndianA;A 4% A;G 40% G;G 56%
  • Luhya (Kenya)A;A 0% A;G 5% G;G 96%
  • Mexican ancestry (Los Angeles)A;A 9% A;G 33% G;G 59%
  • Maasai (Kenya)A;A 2% A;G 15% G;G 83%
  • TuscanA;A 8% A;G 34% G;G 58%

Notes

From SNPedia

Show notes, about 130 words

Nephrolithiasis is a common nephrologic disorder with complex etiology. To identify the genetic factor(s) for nephrolithiasis, we conducted a three-stage genome-wide association study (GWAS) using a total of 5,892 nephrolithiasis cases and 17,809 controls of Japanese origin. Here we found three novel loci for nephrolithiasis: RGS14-SLC34A1-PFN3-F12 on 5q35.3 (rs11746443; P = 8.51×10−12, odds ratio (OR) = 1.19), INMT-FAM188B-AQP1 on 7p14.3 (rs1000597; P = 2.16×10−14, OR = 1.22), and DGKH on 13q14.1 (rs4142110; P = 4.62×10−9, OR = 1.14). Subsequent analyses in 21,842 Japanese subjects revealed the association of SNP rs11746443 with the reduction of estimated glomerular filtration rate (eGFR) (P = 6.54×10−8), suggesting a crucial role for this variation in renal function.

Source and license

Adapted from rs11746443 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.