0 71213Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple1China (ByteDance, Huawei, Baidu…)0Others3Total7Counted 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 T allele shifted the measure 0.08 higher (95% confidence interval 0.057-0.103); p = 6 × 10−13.
How common The T allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 19, band 19p13.13 — a synonymous change in BEST2.
What each result means
C/CNo copy of the version the research linked to Mean corpuscular volume (UKB data field 30040). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Mean corpuscular volume (UKB data field 30040). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Mean corpuscular volume (UKB data field 30040). 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 rs137957583
What is rs137957583?
rs137957583 is a single position in the genome, in or near the BEST2 gene. Published research associates it with mean corpuscular volume (ukb data field 30040). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs137957583 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 rs137957583 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 rs137957583 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 71213Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple1China (ByteDance, Huawei, Baidu…)0Others3Total7Counted 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 (UKB data field 30040) (rs137957583). MyGeneLog™. https://www.mygenelog.com/variants/rs137957583