Solute carrier family 22 member 16 levels (SLC22A16.9969.8.3)
F5 · rs966751
0 7124Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others4Total7Counted 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 3,301 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.45 lower (95% confidence interval -0.35--0.55); p = 5 × 10−17.
How common The G allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 1, band 1q24.2 — in an intron of F5.
What each result means
C/CNo copy of the version the research linked to Solute carrier family 22 member 16 levels (SLC22A16.9969.8.3). This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Solute carrier family 22 member 16 levels (SLC22A16.9969.8.3). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Solute carrier family 22 member 16 levels (SLC22A16.9969.8.3). That is the strongest link of the three results. A link in a study is not a diagnosis.
rs966751 is a single position in the genome, in or near the F5 gene. Published research associates it with solute carrier family 22 member 16 levels (slc22a16.9969.8.3). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does rs966751 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 rs966751 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 rs966751 come from?
GWAS Catalog, Nature 2018, PMID:29875488. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 7124Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others4Total7Counted 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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Solute carrier family 22 member 16 levels (SLC22A16.9969.8.3) (rs966751). MyGeneLog™. https://www.mygenelog.com/variants/rs966751