Standard

Blood protein levels

STK4 · rs35017113

What the study found

Who was studied 3,200 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.229 higher (95% confidence interval 0.16-0.29); p = 5 × 10−12.

How common The C allele had a frequency of about 84% in the people studied.

Where it sits Chromosome 20, band 20q13.12 — in an intron of STK4.

What each result means

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

Questions about rs35017113

What is rs35017113?

rs35017113 is a single position in the genome, in or near the STK4 gene. Published research associates it with blood protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs35017113 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 rs35017113 come from?

GWAS Catalog, Science (New York, N.Y.) 2018, PMID:30072576. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Blood protein levels (rs35017113). MyGeneLog™. https://www.mygenelog.com/variants/rs35017113

← See all variants