High light scatter reticulocyte percentage of red cells
PNKD · rs10716631
0 19171226Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI7Microsoft · Copilot1Amazon2Apple2Others6Total19Counted 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 170,763 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0314 (percentage) lower (95% confidence interval 0.024-0.039); p = 4 × 10−17.
How common The G allele had a frequency of about 54% in the people studied.
Where it sits Chromosome 2, band 2q35 — in an intron of PNKD.
What each result means
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of High light scatter reticulocyte percentage of red cells compared to the general population.
G/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with High light scatter reticulocyte percentage of red cells.
T/TPublished research associates this genotype with typical/baseline likelihood of High light scatter reticulocyte percentage of red cells — no copies of the reported risk allele.
rs10716631 is a single position in the genome, in or near the PNKD gene. Published research associates it with high light scatter reticulocyte percentage of red cells. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs10716631 linked to?
On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.
Does having rs10716631 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 rs10716631 come from?
GWAS Catalog, Cell 2016, PMID:27863252. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 19171226Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI7Microsoft · Copilot1Amazon2Apple2Others6Total19Counted 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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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.
High light scatter reticulocyte percentage of red cells (rs10716631). MyGeneLog™. https://www.mygenelog.com/variants/rs10716631