0 12237Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others7Total12Counted 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 394,642 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.143 lower (95% confidence interval 0.13-0.15); p = 1 × 10−165.
How common The C allele had a frequency of about 3% in the people studied.
Where it sits Chromosome 8, band 8p21.3 — between genes, 14.7 kb from LPL.
What each result means
C/CTwo copies of the version the research linked to Haematocrit percentage (UKB data field 30030). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Haematocrit percentage (UKB data field 30030). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Haematocrit percentage (UKB data field 30030). This is the starting point the study compared everyone against.
Nature genetics · 2025 · PMID 39789286 · open access
Questions about rs75902744
What is rs75902744?
rs75902744 is a single position in the genome, in or near the near LPL gene. Published research associates it with haematocrit percentage (ukb data field 30030). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs75902744 linked to?
On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs75902744 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 rs75902744 come from?
GWAS Catalog, Nature genetics 2025, PMID:39789286. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 12237Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others7Total12Counted 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.
Haematocrit percentage (UKB data field 30030) (rs75902744). MyGeneLog™. https://www.mygenelog.com/variants/rs75902744