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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 416 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 1.83 lower (95% confidence interval 1.29-2.38); p = 2 × 10−10.
How common The G allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 1, band 1q31.3 — a missense change in CFHR2.
What each result means
A/ANo copy of the version the research linked to Complement factor H-related protein 2 levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Complement factor H-related protein 2 levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Complement factor H-related protein 2 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
American journal of human genetics · 2021 · PMID 34260947 · open access
Questions about rs41310132
What is rs41310132?
rs41310132 is a single position in the genome, in or near the CFHR2 gene. Published research associates it with complement factor h-related protein 2 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs41310132 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 rs41310132 come from?
GWAS Catalog, American journal of human genetics 2021, PMID:34260947. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Quoting this page
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Complement factor H-related protein 2 levels (rs41310132). MyGeneLog™. https://www.mygenelog.com/variants/rs41310132