rs1169305

A SNP in the HNF1A gene on chromosome 12. Its most notable genotype is A;G: associated with MODY3; maturity onset of diabetes in the young (type 3)

Gene
HNF1A
Location
Chr 12120,999,579 (GRCh38)
Highest magnitude
2.0Worth knowing
Tested on
23andMe, AncestryDNA
Minor allele frequency
<1%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GGoodcommon in complete genomicsTypical · 0.096% of people
  2. A;GMost notableBadassociated with MODY3; maturity onset of diabetes in the young (type 3)Worth knowing · 2.04% of people
  3. A;AGoodcommon in clinvarTypical · 0.00% of people

SNPedia records rs1169305 on the minus strand: (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 4 HapMap populations.

  • AverageG;G 96% A;G 4% A;A 0%
  • European ancestry (Utah)G;G 100% A;G 0% A;A 0%
  • Han Chinese (Beijing)G;G 100% A;G 0% A;A 0%
  • Japanese (Tokyo)G;G 100% A;G 0% A;A 0%
  • Yoruba (Nigeria)G;G 83% A;G 18% A;A 0%

Notes

From SNPedia

Notes

now considered benign in ClinVar

Source and license

Adapted from rs1169305 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.