Heart rate variability (corrected root mean square of successive differences)
near NDUFA11 · rs35952442
0 826Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others6Total8Counted 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 46,075 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.083 lower (95% confidence interval 0.071-0.095); p = 6 × 10−56.
Where it sits Chromosome 19, band 19p13.3 — between genes, 2.1 kb from NDUFA11.
What each result means
C/CNo copy of the version the research linked to Heart rate variability (corrected root mean square of successive differences). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Heart rate variability (corrected root mean square of successive differences). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Heart rate variability (corrected root mean square of successive differences). That is the strongest link of the three results. A link in a study is not a diagnosis.
Communications biology · 2023 · PMID 37803156 · open access
Questions about rs35952442
What is rs35952442?
rs35952442 is a single position in the genome, in or near the near NDUFA11 gene. Published research associates it with heart rate variability (corrected root mean square of successive differences). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs35952442 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 rs35952442 come from?
GWAS Catalog, Communications biology 2023, PMID:37803156. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 826Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others6Total8Counted 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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Heart rate variability (corrected root mean square of successive differences) (rs35952442). MyGeneLog™. https://www.mygenelog.com/variants/rs35952442