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Complement component C7 levels

C7 · rs74480769

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 1.21 higher (95% confidence interval 1.13-1.28); p = 3 × 10−213.

How common The A allele had a frequency of about 97% in the people studied.

Where it sits Chromosome 5, band 5p13.1 — in an intron of C7.

What each result means

A/A Two copies of the version the research linked to Complement component C7 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Complement component C7 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Complement component C7 levels. This is the starting point the study compared everyone against.
Source

Questions about rs74480769

What is rs74480769?

rs74480769 is a single position in the genome, in or near the C7 gene. Published research associates it with complement component c7 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs74480769 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 rs74480769 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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 component C7 levels (rs74480769). MyGeneLog™. https://www.mygenelog.com/variants/rs74480769

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