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Serum levels of protein CRIM1

LDHC · rs139946387

What the study found

Who was studied 5,359 Icelandic ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.683 lower (95% confidence interval 0.52-0.85); p = 4 × 10−16.

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

Where it sits Chromosome 11, band 11p15.1 — in an intron of LDHC.

What each result means

A/A Two copies of the version the research linked to Serum levels of protein CRIM1. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Serum levels of protein CRIM1. That is a smaller link than two copies.
G/G No copy of the version the research linked to Serum levels of protein CRIM1. This is the starting point the study compared everyone against.
Source

Questions about rs139946387

What is rs139946387?

rs139946387 is a single position in the genome, in or near the LDHC gene. Published research associates it with serum levels of protein crim1. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs139946387 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 rs139946387 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 CRIM1 (rs139946387). MyGeneLog™. https://www.mygenelog.com/variants/rs139946387

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