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Biliary atresia

SCN1A-AS1 · rs114118902

Where this position leads

Condition: Biliary Atresia

rs114118902 Condition: Biliary Atresia Biliary Atresia Condition rs114118902 rs114118902 SCN1A-AS1

What the study found

Who was studied 811 European ancestry cases, 4,654 European ancestry controls.

The effect Each copy of the G allele carried 3.66 times the odds of Biliary atresia (95% confidence interval 3.22-4.1); p = 7 × 10−9.

Where it sits Chromosome 2, band 2q24.3 — in an intron of SCN1A-AS1.

What each result means

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

Questions about rs114118902

What is rs114118902?

rs114118902 is a single position in the genome, in or near the SCN1A-AS1 gene. Published research associates it with biliary atresia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs114118902 linked to?

On MyGeneLog this position is linked to Biliary Atresia. The research behind each link, and its sources, are set out on that condition page.

Does having rs114118902 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 rs114118902 come from?

GWAS Catalog, Journal of hepatology 2023, PMID:37572794. 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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Biliary atresia (rs114118902). MyGeneLog™. https://www.mygenelog.com/variants/rs114118902

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