Type 2 diabetes (adjusted for BMI) or polycystic ovary syndrome (pleiotropy)
FTO · rs9930501
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Who was studied upto 74,124 type 2 diabetes European ancestry cases, upto 824,006 European ancestry controls without type 2 diabetes, upto 10,074 polycystic ovary syndrome European ancestry cases, upto 103,164 polycystic ovary syndrome European ancestry controls without polycystic ovary syndrome.
The effect
The reported allele is A; the catalogue records no effect size
; p = 6 × 10−15.
How common The A allele had a frequency of about 55% in the people studied.
Where it sits Chromosome 16, band 16q12.2 — in an intron of FTO.
What each result means
A/ATwo copies of the version the research linked to Type 2 diabetes (adjusted for BMI) or polycystic ovary syndrome (pleiotropy). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Type 2 diabetes (adjusted for BMI) or polycystic ovary syndrome (pleiotropy). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Type 2 diabetes (adjusted for BMI) or polycystic ovary syndrome (pleiotropy). This is the starting point the study compared everyone against.
rs9930501 is a single position in the genome, in or near the FTO gene. Published research associates it with type 2 diabetes (adjusted for bmi) or polycystic ovary syndrome (pleiotropy). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs9930501 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.
Does having rs9930501 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 rs9930501 come from?
GWAS Catalog, Diabetologia 2022, PMID:35771237. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 61212Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others2Total6Counted 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.
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Type 2 diabetes (adjusted for BMI) or polycystic ovary syndrome (pleiotropy) (rs9930501). MyGeneLog™. https://www.mygenelog.com/variants/rs9930501