Sensitive

Autoimmune thyroid disease

WISP · rs13250295

Where this position leads

Condition: Autoimmune Thyroid Disease

rs13250295 Condition: Autoimmune Thyroid Disease Autoimmune Thyroid Disease Condition rs13250295 rs13250295 WISP

What the study found

Who was studied 30,234 European ancestry cases, 724,172 European ancestry controls.

The effect Each copy of the C allele carried 1.06 times the odds of Autoimmune thyroid disease; p = 8 × 10−12.

How common The C allele had a frequency of about 70% in the people studied.

Where it sits Chromosome 8, band 8q24.22 — in an intron of CCN4.

What each result means

C/C Two copies of the version the research linked to Autoimmune thyroid 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 Autoimmune thyroid disease. That is a smaller link than two copies.
T/T No copy of the version the research linked to Autoimmune thyroid disease. This is the starting point the study compared everyone against.
Source

Questions about rs13250295

What is rs13250295?

rs13250295 is a single position in the genome, in or near the WISP gene. Published research associates it with autoimmune thyroid 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 rs13250295 linked to?

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

Does having rs13250295 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 rs13250295 come from?

GWAS Catalog, Nature 2020, PMID:32581359. 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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Autoimmune thyroid disease (rs13250295). MyGeneLog™. https://www.mygenelog.com/variants/rs13250295

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