Ideal cardiovascular health score (clinical and behavioral)
NFAT5 · rs244417
0 725Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others5Total7Counted 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 119,129 European ancestry individuals, 16,495 African American individuals, 6,780 Hispanic individuals; replicated in 37,646 European ancestry individuals, 5,366 African American individuals, 2,754 Hispanic individuals.
The effect
Each copy of the C allele shifted the measure 0.05 higher; p = 5 × 10−16.
How common The C allele had a frequency of about 39% in the people studied.
Where it sits Chromosome 16, band 16q22.1 — in an intron of NFAT5.
What each result means
C/CTwo copies of the version the research linked to Ideal cardiovascular health score (clinical and behavioral). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Ideal cardiovascular health score (clinical and behavioral). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Ideal cardiovascular health score (clinical and behavioral). This is the starting point the study compared everyone against.
rs244417 is a single position in the genome, in or near the NFAT5 gene. Published research associates it with ideal cardiovascular health score (clinical and behavioral). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs244417 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 rs244417 come from?
GWAS Catalog, PloS one 2022, PMID:35613103. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 725Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others5Total7Counted 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.
Ideal cardiovascular health score (clinical and behavioral) (rs244417). MyGeneLog™. https://www.mygenelog.com/variants/rs244417