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ADGRE1 protein levels

near RN7SL51P · rs13397052

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0703 higher (95% confidence interval 0.059-0.082); p = 6 × 10−38.

How common The G allele had a frequency of about 61% in the people studied.

Where it sits Chromosome 2, band 2p15 — between genes, 56.2 kb from RN7SL51P.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of ADGRE1 protein levels — no copies of the reported risk allele.
C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with ADGRE1 protein levels.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of ADGRE1 protein levels compared to the general population.
Source

Questions about rs13397052

What is rs13397052?

rs13397052 is a single position in the genome, in or near the near RN7SL51P gene. Published research associates it with adgre1 protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13397052 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 rs13397052 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.

ADGRE1 protein levels (rs13397052). MyGeneLog™. https://www.mygenelog.com/variants/rs13397052

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