0 17211229Reads by AI crawlersClaude0ChatGPT2Google · Gemini1Perplexity0Meta AI0Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others9Total17Counted 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 764 Hispanic, European, Asian, South Asian or African American individuals.
The effect
Each copy of the C allele shifted the measure 0.53 lower (95% confidence interval 0.43-0.63); p = 9 × 10−21.
How common The C allele had a frequency of about 8% in the people studied.
Where it sits Chromosome 3, band 3p24.3 — in an intron of PLCL2.
What each result means
A/ANo copy of the version the research linked to Neonatal cytokine/chemokine levels (fetal genetic effect). This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Neonatal cytokine/chemokine levels (fetal genetic effect). That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Neonatal cytokine/chemokine levels (fetal genetic effect). That is the strongest link of the three results. A link in a study is not a diagnosis.
Genome medicine · 2018 · PMID 30134952 · open access
Questions about rs75885714
What is rs75885714?
rs75885714 is a single position in the genome, in or near the PLCL2 gene. Published research associates it with neonatal cytokine/chemokine levels (fetal genetic effect). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs75885714 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 rs75885714 come from?
GWAS Catalog, Genome Med 2018, PMID:30134952. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 17211229Reads by AI crawlersClaude0ChatGPT2Google · Gemini1Perplexity0Meta AI0Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others9Total17Counted 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.