Mental health study participation (provided email address)
RP11-436D23.1 · rs10499016
0 00Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others0Total0Counted 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 224,321 British ancestry cases, 147,096 British ancestry controls.
The effect
Each copy of the G allele shifted the measure 0.00815 lower (95% confidence interval 0.0053-0.011); p = 2 × 10−8.
Where it sits Chromosome 6, band 6q16.1 — between genes, 50.4 kb from EIF4EBP2P3.
What each result means
A/ANo copy of the version the research linked to Mental health study participation (provided email address). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Mental health study participation (provided email address). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Mental health study participation (provided email address). 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 rs10499016
What is rs10499016?
rs10499016 is a single position in the genome, in or near the RP11-436D23.1 gene. Published research associates it with mental health study participation (provided email address). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10499016 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 rs10499016 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.
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Quoting this page
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Mental health study participation (provided email address) (rs10499016). MyGeneLog™. https://www.mygenelog.com/variants/rs10499016