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C1QTNF9 protein levels

RNF17 · rs191501886

Where this position leads

Condition: Celiac Disease

rs191501886 Condition: Celiac Disease Celiac Disease Condition rs191501886 rs191501886 RNF17

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.228 lower (95% confidence interval 0.16-0.3); p = 8 × 10−12.

How common The G allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 13, band 13q12.12 — in an intron of RNF17.

What each result means

A/A No copy of the version the research linked to C1QTNF9 protein levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to C1QTNF9 protein levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to C1QTNF9 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs191501886

What is rs191501886?

rs191501886 is a single position in the genome, in or near the RNF17 gene. Published research associates it with c1qtnf9 protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs191501886 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 rs191501886 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 rs191501886 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.

C1QTNF9 protein levels (rs191501886). MyGeneLog™. https://www.mygenelog.com/variants/rs191501886

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