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Complement factor H-related protein 4A levels

CFH · rs10922108

What the study found

Who was studied 416 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.449 lower (95% confidence interval 0.35-0.55); p = 3 × 10−16.

How common The T allele had a frequency of about 34% in the people studied.

Where it sits Chromosome 1, band 1q31.3 — in an intron of CFH.

What each result means

A/A No copy of the version the research linked to Complement factor H-related protein 4A levels. This is the starting point the study compared everyone against.
A/T One copy of the version the research linked to Complement factor H-related protein 4A levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Complement factor H-related protein 4A levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs10922108

What is rs10922108?

rs10922108 is a single position in the genome, in or near the CFH gene. Published research associates it with complement factor h-related protein 4a levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10922108 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 rs10922108 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.

Quoting this page

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Complement factor H-related protein 4A levels (rs10922108). MyGeneLog™. https://www.mygenelog.com/variants/rs10922108

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