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Serum levels of protein ACHE

near RN7SL549P · rs4727469

What the study found

Who was studied 5,363 Icelandic ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.299 higher (95% confidence interval 0.26-0.33); p = 3 × 10−60.

How common The T allele had a frequency of about 47% in the people studied.

Where it sits Chromosome 7, band 7q22.1 — between genes, 5 kb from RN7SL549P.

What each result means

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

Questions about rs4727469

What is rs4727469?

rs4727469 is a single position in the genome, in or near the near RN7SL549P gene. Published research associates it with serum levels of protein ache. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4727469 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 rs4727469 come from?

GWAS Catalog, Nature communications 2022, PMID:35078996. 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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Serum levels of protein ACHE (rs4727469). MyGeneLog™. https://www.mygenelog.com/variants/rs4727469

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