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HIV setpoint viral load

CCR5AS · rs7637813

What the study found

Who was studied 7,890 European and African ancestry males.

The effect Each copy of the G allele shifted the measure 0.19 lower (95% confidence interval 0.15-0.23); p = 6 × 10−21.

Where it sits Chromosome 3, band 3p21.31 — in an intron of CCR5AS.

What each result means

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

Questions about rs7637813

What is rs7637813?

rs7637813 is a single position in the genome, in or near the CCR5AS gene. Published research associates it with hiv setpoint viral load. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7637813 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 rs7637813 come from?

GWAS Catalog, JCI insight 2023, PMID:37097752. 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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HIV setpoint viral load (rs7637813). MyGeneLog™. https://www.mygenelog.com/variants/rs7637813

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