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Collectin-10 levels

LINC01322 · rs17713196

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.272 higher (95% confidence interval 0.24-0.3); p = 2 × 10−61.

How common The T allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 3, band 3q26.1 — in an intron of LINC01322.

What each result means

C/C No copy of the version the research linked to Collectin-10 levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Collectin-10 levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Collectin-10 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs17713196

What is rs17713196?

rs17713196 is a single position in the genome, in or near the LINC01322 gene. Published research associates it with collectin-10 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17713196 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 rs17713196 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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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Collectin-10 levels (rs17713196). MyGeneLog™. https://www.mygenelog.com/variants/rs17713196

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