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Atrial fibrillation

SCN10A · rs6790396

Where this position leads

Condition: Atrial Fibrillation

rs6790396 Condition: Atrial Fibrillation Atrial Fibrillation Condition rs6790396 rs6790396 SCN10A

What the study found

Who was studied 60,620 European ancestry cases, 970,216 European ancestry controls.

The effect Each copy of the G allele carried 1.06 times the odds of Atrial fibrillation (95% confidence interval 1.05-1.08); p = 2 × 10−20.

How common The G allele had a frequency of about 60% in the people studied.

Where it sits Chromosome 3, band 3p22.2 — in an intron of SCN10A.

What each result means

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

Questions about rs6790396

What is rs6790396?

rs6790396 is a single position in the genome, in or near the SCN10A gene. Published research associates it with atrial fibrillation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs6790396 linked to?

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

Does having rs6790396 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 rs6790396 come from?

GWAS Catalog, Nat Genet 2018, PMID:30061737. 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.

Atrial fibrillation (rs6790396). MyGeneLog™. https://www.mygenelog.com/variants/rs6790396

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