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Mannan-binding lectin serine protease 1 levels

near ZNF385B · rs259842

What the study found

Who was studied 997 European ancestry individuals; replicated in 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.351 higher (95% confidence interval 0.26-0.44); p = 4 × 10−15.

Where it sits Chromosome 2, band 2q31.3 — between genes, 12.5 kb from ZNF385B.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Mannan-binding lectin serine protease 1 levels — 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 Mannan-binding lectin serine protease 1 levels.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Mannan-binding lectin serine protease 1 levels compared to the general population.
Source

Questions about rs259842

What is rs259842?

rs259842 is a single position in the genome, in or near the near ZNF385B gene. Published research associates it with mannan-binding lectin serine protease 1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs259842 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 rs259842 come from?

GWAS Catalog, Nature communications 2017, PMID:28240269. 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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Mannan-binding lectin serine protease 1 levels (rs259842). MyGeneLog™. https://www.mygenelog.com/variants/rs259842

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