0 00Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0Others0Total0Counted 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 74,049 African American or Afro-Caribbean individuals, 37,043 Hispanic or Latin American individuals, 3,003 East Asian ancestry individuals, 275,068 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0421 lower (95% confidence interval 0.03-0.055); p = 4 × 10−11.
How common The A allele had a frequency of about 92% in the people studied.
Where it sits Chromosome 1, band 1p31.1 — in an intron of SLC44A5.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of neutrophil (absolute count, minimum, inv-norm transformed) compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with neutrophil (absolute count, minimum, inv-norm transformed).
G/GPublished research associates this genotype with typical/baseline likelihood of neutrophil (absolute count, minimum, inv-norm transformed) — no copies of the reported risk allele.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs1249662
What is rs1249662?
rs1249662 is a single position in the genome, in or near the SLC44A5 gene. Published research associates it with neutrophil (absolute count, minimum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1249662 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 rs1249662 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 00Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0Others0Total0Counted 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.