0 30221712312Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity1Meta AI7Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others12Total30Counted 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.
Who was studied 382,500 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0207 higher (95% confidence interval 0.014-0.028); p = 3 × 10−9.
How common The C allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 11, band 11p15.4 — in an intron of SBF2.
What each result means
C/CTwo copies of the version the research linked to Urinary albumin excretion. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Urinary albumin excretion. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Urinary albumin excretion. This is the starting point the study compared everyone against.
American journal of human genetics · 2018 · PMID 30220432
Questions about rs17368443
What is rs17368443?
rs17368443 is a single position in the genome, in or near the SBF2 gene. Published research associates it with urinary albumin excretion. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs17368443 linked to?
On MyGeneLog this position is linked to Kidney Function. The research behind each link, and its sources, are set out on that condition page.
Does having rs17368443 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 rs17368443 come from?
GWAS Catalog, Am J Hum Genet 2018, PMID:30220432. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 30221712312Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity1Meta AI7Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others12Total30Counted 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.
Urinary albumin excretion (rs17368443). MyGeneLog™. https://www.mygenelog.com/variants/rs17368443