0 1722211Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others11Total17Counted 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 71,019 Korean ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0828 lower (95% confidence interval 0.069-0.097); p = 8 × 10−31.
How common The A allele had a frequency of about 12% in the people studied.
Where it sits Chromosome 7, band 7p15.3 — inside STEAP1B.
What each result means
A/ATwo copies of the version the research linked to High-sensitivity C-reactive protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to High-sensitivity C-reactive protein levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to High-sensitivity C-reactive protein levels. This is the starting point the study compared everyone against.
Scientific reports · 2025 · PMID 39747571 · open access
Questions about rs78821961
What is rs78821961?
rs78821961 is a single position in the genome, in or near the STEAP1B gene. Published research associates it with high-sensitivity c-reactive protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs78821961 linked to?
On MyGeneLog this position is linked to C-Reactive Protein Levels. The research behind each link, and its sources, are set out on that condition page.
Does having rs78821961 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 rs78821961 come from?
GWAS Catalog, Scientific reports 2025, PMID:39747571. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 1722211Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others11Total17Counted 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.
High-sensitivity C-reactive protein levels (rs78821961). MyGeneLog™. https://www.mygenelog.com/variants/rs78821961