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Serum levels of protein ANXA6

near RN7SL218P · rs16850360

What the study found

Who was studied 5,362 Icelandic ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.587 lower (95% confidence interval 0.47-0.7); p = 4 × 10−23.

How common The G allele had a frequency of about 3% in the people studied.

Where it sits Chromosome 4, band 4q13.3 — between genes, 4.8 kb from RN7SL218P.

What each result means

A/A No copy of the version the research linked to Serum levels of protein ANXA6. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Serum levels of protein ANXA6. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Serum levels of protein ANXA6. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs16850360

What is rs16850360?

rs16850360 is a single position in the genome, in or near the near RN7SL218P gene. Published research associates it with serum levels of protein anxa6. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs16850360 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 rs16850360 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 ANXA6 (rs16850360). MyGeneLog™. https://www.mygenelog.com/variants/rs16850360

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