High light scatter reticulocyte count (UKB data field 30300)
LINC01524 · rs4431004
0 121227Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (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 G allele shifted the measure 0.018 lower (95% confidence interval 0.014-0.022); p = 3 × 10−17.
How common The G allele had a frequency of about 29% in the people studied.
Where it sits Chromosome 20, band 20q13.2 — in an intron of LINC01524.
What each result means
A/ANo copy of the version the research linked to High light scatter reticulocyte count (UKB data field 30300). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to High light scatter reticulocyte count (UKB data field 30300). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to High light scatter reticulocyte count (UKB data field 30300). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2025 · PMID 39789286 · open access
Questions about rs4431004
What is rs4431004?
rs4431004 is a single position in the genome, in or near the LINC01524 gene. Published research associates it with high light scatter reticulocyte count (ukb data field 30300). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs4431004 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 rs4431004 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 rs4431004 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 121227Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (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.
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High light scatter reticulocyte count (UKB data field 30300) (rs4431004). MyGeneLog™. https://www.mygenelog.com/variants/rs4431004