Sensitive

Myocardial infarction

RNF13 · rs41411047

Where this position leads

Condition: Myocardial Infarction

rs41411047 Condition: Myocardial Infarction Myocardial Infarction Condition rs41411047 rs41411047 RNF13

What the study found

Who was studied 2,563 Saudi Arab ancestry cases, 1,868 Saudi Arab ancestry controls; replicated in 866 Saudi Arab ancestry cases, 371 Saudi Arab ancestry controls.

The effect Each copy of the A allele carried 1.51 times the odds of Myocardial infarction; p = 1 × 10−11.

How common The A allele had a frequency of about 9% in the people studied.

Where it sits Chromosome 3, band 3q25.1 — in an intron of RNF13.

What each result means

A/A Two copies of the version the research linked to Myocardial infarction. 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 Myocardial infarction. That is a smaller link than two copies.
G/G No copy of the version the research linked to Myocardial infarction. This is the starting point the study compared everyone against.
Source

Questions about rs41411047

What is rs41411047?

rs41411047 is a single position in the genome, in or near the RNF13 gene. Published research associates it with myocardial infarction. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs41411047 linked to?

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

Does having rs41411047 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 rs41411047 come from?

GWAS Catalog, Atherosclerosis 2016, PMID:26708285. 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.

Myocardial infarction (rs41411047). MyGeneLog™. https://www.mygenelog.com/variants/rs41411047

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