Sensitive

Coronary artery disease in type 1 diabetes

MAP1B · rs115829748

Where this position leads

Condition: Type 1 Diabetes

rs115829748 Condition: Type 1 Diabetes Type 1 Diabetes Condition rs115829748 rs115829748 MAP1B

What the study found

Who was studied 434 European ancestry cases with coronary artery disease, 3,123 European ancestry cases without coronary artery disease; replicated in 585 cases with coronary artery disease, 2,612 cases without coronary artery disease.

The effect Each copy of the T allele carried 3.16 times the odds of Coronary artery disease in type 1 diabetes; p = 1 × 10−9.

How common The T allele had a frequency of about 4% in the people studied.

Where it sits Chromosome 5, band 5q13.2 — in an intron of LOC105379028.

What each result means

C/C No copy of the version the research linked to Coronary artery disease in type 1 diabetes. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Coronary artery disease in type 1 diabetes. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Coronary artery disease in type 1 diabetes. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs115829748

What is rs115829748?

rs115829748 is a single position in the genome, in or near the MAP1B gene. Published research associates it with coronary artery disease in type 1 diabetes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs115829748 linked to?

On MyGeneLog this position is linked to Type 1 Diabetes. The research behind each link, and its sources, are set out on that condition page.

Does having rs115829748 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 rs115829748 come from?

GWAS Catalog, Cardiovasc Diabetol 2018, PMID:29695241. 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.

Coronary artery disease in type 1 diabetes (rs115829748). MyGeneLog™. https://www.mygenelog.com/variants/rs115829748

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