0 29321622310Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others10Total29Counted 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.
Who was studied 957 European ancestry cases, 12,323 European ancestry controls.
The effect
Each copy of the T allele carried 1.32 times the odds of Type 1 diabetes with low genetic risk score (95% confidence interval 1.203-1.452); p = 6 × 10−9.
Where it sits Chromosome 1, band 1q23.1 — inside OR6N1.
What each result means
C/CNo copy of the version the research linked to Type 1 diabetes with low genetic risk score. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Type 1 diabetes with low genetic risk score. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Type 1 diabetes with low genetic risk score. That is the strongest link of the three results. A link in a study is not a diagnosis.
Communications biology · 2021 · PMID 34302048 · open access
Questions about rs857786
What is rs857786?
rs857786 is a single position in the genome, in or near the MNDA gene. Published research associates it with type 1 diabetes with low genetic risk score. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs857786 linked to?
On MyGeneLog this position is linked to Type 1 Diabetes. The research behind each link, and its sources, are set out on that condition page.
Does having rs857786 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 rs857786 come from?
GWAS Catalog, Commun Biol 2021, PMID:34302048. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 29321622310Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others10Total29Counted 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 1 diabetes with low genetic risk score (rs857786). MyGeneLog™. https://www.mygenelog.com/variants/rs857786