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Percentage of FA2BG1 in total neutral plasma glycans (GPn) (GP63)

SMARCB1 · rs17630758

What the study found

Who was studied 10,172 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.28 lower (95% confidence interval 0.24-0.32); p = 3 × 10−35.

How common The A allele had a frequency of about 16% in the people studied.

Where it sits Chromosome 22, band 22q11.23 — in an intron of SMARCB1.

What each result means

A/A Two copies of the version the research linked to Percentage of FA2BG1 in total neutral plasma glycans (GPn) (GP63). 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 Percentage of FA2BG1 in total neutral plasma glycans (GPn) (GP63). That is a smaller link than two copies.
G/G No copy of the version the research linked to Percentage of FA2BG1 in total neutral plasma glycans (GPn) (GP63). This is the starting point the study compared everyone against.
Source

Questions about rs17630758

What is rs17630758?

rs17630758 is a single position in the genome, in or near the SMARCB1 gene. Published research associates it with percentage of fa2bg1 in total neutral plasma glycans (gpn) (gp63). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17630758 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 rs17630758 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.

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Percentage of FA2BG1 in total neutral plasma glycans (GPn) (GP63) (rs17630758). MyGeneLog™. https://www.mygenelog.com/variants/rs17630758

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