Sensitive

Graves' disease

MHC · rs4248154

Where this position leads

Condition: Graves' Disease

rs4248154 Condition: Graves' Disease Graves' Disease Condition rs4248154 rs4248154 MHC

What the study found

Who was studied 1,119 Japanese ancestry cases, 2,718 Japanese ancestry controls; replicated in 432 Japanese ancestry cases, 1,157 Japanese ancestry controls.

The effect Each copy of the C allele carried 1.38 times the odds of Graves' disease (95% confidence interval 1.27-1.50); p = 1 × 10−13.

How common The C allele had a frequency of about 54% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — a synonymous change in MUC22.

What each result means

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

Questions about rs4248154

What is rs4248154?

rs4248154 is a single position in the genome, in or near the MHC gene. Published research associates it with graves' disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs4248154 linked to?

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

Does having rs4248154 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 rs4248154 come from?

GWAS Catalog, J Hum Genet 2011, PMID:21900946. 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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Graves' disease (rs4248154). MyGeneLog™. https://www.mygenelog.com/variants/rs4248154

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