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Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.
What the study found
Who was studied 4,549 European ancestry cases, 5,579 European ancestry controls; replicated in 24,194 European ancestry cases, 55,598 European ancestry controls.
The effect
Each copy of the T allele carried 1.13 times the odds of Type 2 diabetes (95% confidence interval 1.08-1.17); p = 4 × 10−8.
How common The T allele had a frequency of about 11% in the people studied.
Where it sits Chromosome 1, band 1p12 — in an intron of NOTCH2.
What each result means
G/GNo copy of the version the research linked to Type 2 diabetes. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Type 2 diabetes. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Type 2 diabetes. That is the strongest link of the three results. A link in a study is not a diagnosis.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs10923931
What is rs10923931?
rs10923931 is a single position in the genome, in or near the NOTCH2 gene. Published research associates it with type 2 diabetes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs10923931 linked to?
On MyGeneLog this position is linked to Type 2 Diabetes. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs10923931?
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (12 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs10923931 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs10923931 come from?
GWAS Catalog, Nat Genet 2008, PMID:18372903. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 6252439222231Reads by AI crawlersClaude5ChatGPT2Google · Gemini4Perplexity3Meta AI9Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others31Total62Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Type 2 diabetes (rs10923931). MyGeneLog™. https://www.mygenelog.com/variants/rs10923931