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Serum levels of protein NOG

SUFU · rs12767683

What the study found

Who was studied 5,366 Icelandic ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.227 higher (95% confidence interval 0.18-0.27); p = 1 × 10−25.

How common The A allele had a frequency of about 26% in the people studied.

Where it sits Chromosome 10, band 10q24.32 — in an intron of SUFU.

What each result means

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

Questions about rs12767683

What is rs12767683?

rs12767683 is a single position in the genome, in or near the SUFU gene. Published research associates it with serum levels of protein nog. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12767683 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 rs12767683 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 NOG (rs12767683). MyGeneLog™. https://www.mygenelog.com/variants/rs12767683

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