Sulfotransferase family cytosolic 1B member 1 levels
F5 · rs6663533
0 18112212Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others12Total18Counted 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 10,708 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.644 lower (95% confidence interval 0.59-0.7); p = 4 × 10−116.
How common The T allele had a frequency of about 94% in the people studied.
Where it sits Chromosome 1, band 1q24.2 — in an intron of F5.
What each result means
G/GNo copy of the version the research linked to Sulfotransferase family cytosolic 1B member 1 levels. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Sulfotransferase family cytosolic 1B member 1 levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Sulfotransferase family cytosolic 1B member 1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs6663533 is a single position in the genome, in or near the F5 gene. Published research associates it with sulfotransferase family cytosolic 1b member 1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does rs6663533 affect how medicines work?
F5 carries pharmacogenomic findings for Combined hormonal contraceptives. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.
Does having rs6663533 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 rs6663533 come from?
GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 18112212Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others12Total18Counted 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.
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Sulfotransferase family cytosolic 1B member 1 levels (rs6663533). MyGeneLog™. https://www.mygenelog.com/variants/rs6663533