Standard

Apolipoprotein A levels (UKB data field 30630)

near LNC-RHL1 · rs189391949

Where this position leads

Condition: Celiac Disease

rs189391949 Condition: Celiac Disease Celiac Disease Condition rs189391949 rs189391949 near LNC-RHL1

What the study found

Who was studied 394,642 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.107 higher (95% confidence interval 0.076-0.138); p = 1 × 10−12.

How common The T allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 11, band 11q23.3 — between genes, 2.7 kb from LNC-RHL1.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Apolipoprotein A levels (UKB data field 30630) — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Apolipoprotein A levels (UKB data field 30630).
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Apolipoprotein A levels (UKB data field 30630) compared to the general population.
Source

Questions about rs189391949

What is rs189391949?

rs189391949 is a single position in the genome, in or near the near LNC-RHL1 gene. Published research associates it with apolipoprotein a levels (ukb data field 30630). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs189391949 linked to?

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

Does having rs189391949 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 rs189391949 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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.

Apolipoprotein A levels (UKB data field 30630) (rs189391949). MyGeneLog™. https://www.mygenelog.com/variants/rs189391949

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