Sensitive

Type 2 diabetes

ZRANB3 · rs1465146591

Where this position leads

Condition: Type 2 Diabetes

rs1465146591 Condition: Type 2 Diabetes Type 2 Diabetes Condition rs1465146591 rs1465146591 ZRANB3

What the study found

Who was studied 2,342 Sub-Saharan African ancestry cases, 2,889 Sub-Saharan African ancestry controls; replicated in 1,602 South African Zulu ancestry cases, 976 South African Zulu ancestry controls.

The effect Each copy of the A allele shifted the measure 0.652 lower (95% confidence interval 0.43-0.87); p = 7 × 10−9.

How common The A allele had a frequency of about 7% in the people studied.

Where it sits Chromosome 2, band 2q21.3 — in an intron of ZRANB3.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Type 2 diabetes compared to the general population.
A/C Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Type 2 diabetes.
C/C Published research associates this genotype with typical/baseline likelihood of Type 2 diabetes — no copies of the reported risk allele.
Source

Questions about rs1465146591

What is rs1465146591?

rs1465146591 is a single position in the genome, in or near the ZRANB3 gene. Published research associates it with type 2 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 rs1465146591 linked to?

On MyGeneLog this position is linked to Type 2 Diabetes. The research behind each link, and its sources, are set out on that condition page.

Does having rs1465146591 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 rs1465146591 come from?

GWAS Catalog, Nat Commun 2019, PMID:31324766. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants