Mental health study participation (completed survey)
NTM · rs10791143
0 22Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others2Total2Counted 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.
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 122,647 British ancestry cases, 248,781 British ancestry controls.
The effect
Each copy of the G allele shifted the measure 0.00749 higher (95% confidence interval 0.0053-0.0097); p = 2 × 10−11.
How common The G allele had a frequency of about 62% in the people studied.
Where it sits Chromosome 11, band 11q25 — in an intron of NTM.
What each result means
A/ANo copy of the version the research linked to Mental health study participation (completed survey). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Mental health study participation (completed survey). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Mental health study participation (completed survey). That is the strongest link of the three results. A link in a study is not a diagnosis.
International journal of epidemiology · 2020 · PMID 31263887 · open access
Questions about rs10791143
What is rs10791143?
rs10791143 is a single position in the genome, in or near the NTM gene. Published research associates it with mental health study participation (completed survey). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10791143 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 rs10791143 come from?
GWAS Catalog, International journal of epidemiology 2020, PMID:31263887. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 22Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others2Total2Counted 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
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Mental health study participation (completed survey) (rs10791143). MyGeneLog™. https://www.mygenelog.com/variants/rs10791143