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Cerebrospinal fluid protein GFER levels

near GFER · rs113097793

What the study found

Who was studied 2,524 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.308 higher (95% confidence interval 0.26-0.36); p = 3 × 10−37.

How common The A allele had a frequency of about 17% in the people studied.

Where it sits Chromosome 16, band 16p13.3 — between genes, 0.1 kb from GFER.

What each result means

A/A Two copies of the version the research linked to Cerebrospinal fluid protein GFER 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 Cerebrospinal fluid protein GFER levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Cerebrospinal fluid protein GFER levels. This is the starting point the study compared everyone against.
Source

Questions about rs113097793

What is rs113097793?

rs113097793 is a single position in the genome, in or near the near GFER gene. Published research associates it with cerebrospinal fluid protein gfer levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs113097793 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 rs113097793 come from?

GWAS Catalog, Science translational medicine 2026, PMID:42054495. 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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Cerebrospinal fluid protein GFER levels (rs113097793). MyGeneLog™. https://www.mygenelog.com/variants/rs113097793

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