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TRAIL levels

NCEH1 · rs73173340

Where this position leads

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of TRAIL levels — no copies of the reported risk allele.

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with TRAIL levels.

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of TRAIL levels compared to the general population.

Source

Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors

Ahola-Olli AV, Würtz P, Havulinna AS, Aalto K, Pitkänen N, Lehtimäki T, Kähönen M, Lyytikäinen LP, Raitoharju E, Seppälä I, Sarin AP, Ripatti S

and 9 more — show all

Palotie A, Perola M, Viikari JS, Jalkanen S, Maksimow M, Salomaa V, Salmi M, Kettunen J, Raitakari OT

American journal of human genetics · 2017 · PMID 27989323

Questions about rs73173340

What is rs73173340?

rs73173340 is a single position in the genome, in or near the NCEH1 gene. Published research associates it with trail 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 rs73173340 linked to?

On MyGeneLog this position is linked to MIP-1b (CCL4) Levels. The research behind each link, and its sources, are set out on that condition page.

Does having rs73173340 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 rs73173340 come from?

GWAS Catalog, Am J Hum Genet 2016, PMID:27989323. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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