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Complement factor H-related protein 5 levels

CFHR5 · rs146719763

What the study found

Who was studied 2,935 Qatari ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.935 lower (95% confidence interval 0.72-1.15); p = 5 × 10−18.

How common The C allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 1, band 1q31.3 — in an intron of CFHR5.

What each result means

C/C Two copies of the version the research linked to Complement factor H-related protein 5 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Complement factor H-related protein 5 levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Complement factor H-related protein 5 levels. This is the starting point the study compared everyone against.
Source

Questions about rs146719763

What is rs146719763?

rs146719763 is a single position in the genome, in or near the CFHR5 gene. Published research associates it with complement factor h-related protein 5 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs146719763 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 rs146719763 come from?

GWAS Catalog, Human molecular genetics 2023, PMID:36168886. 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 5 levels (rs146719763). MyGeneLog™. https://www.mygenelog.com/variants/rs146719763

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