0 1922114Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others14Total19Counted 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 362,595 British ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.26 % lower (95% confidence interval -0.28--0.23); p = 8 × 10−88.
How common The C allele had a frequency of about 76% in the people studied.
Where it sits Chromosome 10, band 10q11.21 — between genes, 3.6 kb from MARCHF8.
What each result means
A/ANo copy of the version the research linked to Mean corpuscular volume. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Mean corpuscular volume. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Mean corpuscular volume. That is the strongest link of the three results. A link in a study is not a diagnosis.
Human molecular genetics · 2021 · PMID 34104963 · open access
Questions about rs7089063
What is rs7089063?
rs7089063 is a single position in the genome, in or near the near MARCHF8 gene. Published research associates it with mean corpuscular volume. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7089063 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 rs7089063 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 rs7089063 come from?
GWAS Catalog, Human molecular genetics 2021, PMID:34104963. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 1922114Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others14Total19Counted 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.
Mean corpuscular volume (rs7089063). MyGeneLog™. https://www.mygenelog.com/variants/rs7089063