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Serum levels of protein PCDHGA1

near CD177 · rs12975477

What the study found

Who was studied 5,367 Icelandic ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.58 higher (95% confidence interval 0.41-0.75); p = 4 × 10−11.

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

Where it sits Chromosome 19, band 19q13.31 — between genes, 1.8 kb from CD177.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum levels of protein PCDHGA1 compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum levels of protein PCDHGA1.
G/G Published research associates this genotype with typical/baseline likelihood of Serum levels of protein PCDHGA1 — no copies of the reported risk allele.
Source

Questions about rs12975477

What is rs12975477?

rs12975477 is a single position in the genome, in or near the near CD177 gene. Published research associates it with serum levels of protein pcdhga1. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12975477 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 rs12975477 come from?

GWAS Catalog, Nature communications 2022, PMID:35078996. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Serum levels of protein PCDHGA1 (rs12975477). MyGeneLog™. https://www.mygenelog.com/variants/rs12975477

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