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Its strongest genetic-study result is p = 10−34, with 1 associations in the GWAS Catalog.
How this is scored
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 630,125 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals.
The effect
The reported allele is G; the catalogue records no effect size
; p = 1 × 10−34.
How common The G allele had a frequency of about 31% in the people studied.
Where it sits Chromosome 1, band 1p31.3 — between genes, 51.8 kb from LEPR.
What each result means
A/ANo copy of the version the research linked to Mean corpuscular hemoglobin. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Mean corpuscular hemoglobin. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Mean corpuscular hemoglobin. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs11208719 is a single position in the genome, in or near the near LEPR gene. Published research associates it with mean corpuscular hemoglobin. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11208719 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 rs11208719 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 rs11208719 come from?
GWAS Catalog, Cell 2020, PMID:32888493. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 21215238Reads by AI crawlersClaude0ChatGPT0Google · Gemini2Perplexity1Meta AI0Microsoft · Copilot5Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others8Total21Counted 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 hemoglobin (rs11208719). MyGeneLog™. https://www.mygenelog.com/variants/rs11208719