Sensitive

Decreased low contrast letter acuity in multiple sclerosis

MSI2 · rs72830848

Where this position leads

Condition: Multiple Sclerosis

rs72830848 Condition: Multiple Sclerosis Multiple Sclerosis Condition rs72830848 rs72830848 MSI2

What the study found

Who was studied 582 European and unknown ancestry individuals; replicated in 253 European and unknown ancestry individuals.

The effect Each copy of the T allele carried 2.25 times the odds of Decreased low contrast letter acuity in multiple sclerosis (95% confidence interval 1.78-2.85); p = 4 × 10−8.

How common The T allele had a frequency of about 6% in the people studied.

Where it sits Chromosome 17, band 17q22 — in an intron of MSI2.

What each result means

C/C No copy of the version the research linked to Decreased low contrast letter acuity in multiple sclerosis. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Decreased low contrast letter acuity in multiple sclerosis. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Decreased low contrast letter acuity in multiple sclerosis. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs72830848

What is rs72830848?

rs72830848 is a single position in the genome, in or near the MSI2 gene. Published research associates it with decreased low contrast letter acuity in multiple sclerosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs72830848 linked to?

On MyGeneLog this position is linked to Multiple Sclerosis. The research behind each link, and its sources, are set out on that condition page.

Does having rs72830848 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 rs72830848 come from?

GWAS Catalog, Brain : a journal of neurology 2019, PMID:31289819. 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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Decreased low contrast letter acuity in multiple sclerosis (rs72830848). MyGeneLog™. https://www.mygenelog.com/variants/rs72830848

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