0 826Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others6Total8Counted 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 5,366 Icelandic ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.12 lower (95% confidence interval 0.081-0.159); p = 1 × 10−9.
How common The A allele had a frequency of about 32% in the people studied.
Where it sits Chromosome 15, band 15q21.2 — in an intron of FAM227B.
What each result means
A/ATwo copies of the version the research linked to Serum levels of protein FGF7. 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 Serum levels of protein FGF7. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Serum levels of protein FGF7. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 35078996 · open access
Questions about rs1911612
What is rs1911612?
rs1911612 is a single position in the genome, in or near the FAM227B gene. Published research associates it with serum levels of protein fgf7. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1911612 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 rs1911612 come from?
GWAS Catalog, Nature communications 2022, PMID:35078996. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 826Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others6Total8Counted 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.
Serum levels of protein FGF7 (rs1911612). MyGeneLog™. https://www.mygenelog.com/variants/rs1911612