Neonatal circulating Complement Component 4 (C4) protein concentration
VARS1 · rs11751198
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 68,768 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.39 higher (95% confidence interval 0.35-0.43); p = 8 × 10−145.
Where it sits Chromosome 6, band 6p21.33 — inside VARS1.
What each result means
A/ATwo copies of the version the research linked to Neonatal circulating Complement Component 4 (C4) protein concentration. 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 Neonatal circulating Complement Component 4 (C4) protein concentration. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Neonatal circulating Complement Component 4 (C4) protein concentration. This is the starting point the study compared everyone against.
Cell genomics · 2023 · PMID 38116117 · open access
Questions about rs11751198
What is rs11751198?
rs11751198 is a single position in the genome, in or near the VARS1 gene. Published research associates it with neonatal circulating complement component 4 (c4) protein concentration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11751198 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 rs11751198 come from?
GWAS Catalog, Cell genomics 2023, PMID:38116117. 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.
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