0 5122Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot1Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total5Counted 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 116,285 African American or Afro-Caribbean individuals, 57,003 Hispanic or Latin American individuals, 6,275 East Asian ancestry individuals, 420,576 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0279 lower (95% confidence interval 0.021-0.035); p = 4 × 10−16.
How common The T allele had a frequency of about 85% in the people studied.
Where it sits Chromosome 2, band 2p16.2 — in a non-coding transcript of SPTBN1.
What each result means
C/CNo copy of the version the research linked to creatinine (maximum, inv-norm transformed). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to creatinine (maximum, inv-norm transformed). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to creatinine (maximum, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs62134679
What is rs62134679?
rs62134679 is a single position in the genome, in or near the SPTBN1 gene. Published research associates it with creatinine (maximum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs62134679 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 rs62134679 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 5122Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot1Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total5Counted 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.