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Percentage of FA2G1 in total neutral plasma glycans (GPn) (GP61)

near RUNX3 · rs10903118

What the study found

Who was studied 10,172 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.105 lower (95% confidence interval 0.074-0.136); p = 3 × 10−11.

How common The C allele had a frequency of about 51% in the people studied.

Where it sits Chromosome 1, band 1p36.11 — between genes, 3.3 kb from RUNX3.

What each result means

C/C Two copies of the version the research linked to Percentage of FA2G1 in total neutral plasma glycans (GPn) (GP61). 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 Percentage of FA2G1 in total neutral plasma glycans (GPn) (GP61). That is a smaller link than two copies.
T/T No copy of the version the research linked to Percentage of FA2G1 in total neutral plasma glycans (GPn) (GP61). This is the starting point the study compared everyone against.
Source

Questions about rs10903118

What is rs10903118?

rs10903118 is a single position in the genome, in or near the near RUNX3 gene. Published research associates it with percentage of fa2g1 in total neutral plasma glycans (gpn) (gp61). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10903118 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 rs10903118 come from?

GWAS Catalog, Nature communications 2025, PMID:40593539. 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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Percentage of FA2G1 in total neutral plasma glycans (GPn) (GP61) (rs10903118). MyGeneLog™. https://www.mygenelog.com/variants/rs10903118

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