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Hypothyroidism

RASGRP1 · rs12593201

Where this position leads

Condition: Hypothyroidism

rs12593201 Condition: Hypothyroidism Hypothyroidism Condition rs12593201 rs12593201 RASGRP1

What the study found

Who was studied 30,155 European ancestry cases, 379,986 European ancestry controls, 1,114 East Asian ancestry cases, 172,656 East Asian ancestry controls.

The effect Each copy of the A allele shifted the measure 0.0905 higher (95% confidence interval 0.069-0.112); p = 8 × 10−16.

Where it sits Chromosome 15, band 15q14 — in an intron of RASGRP1.

What each result means

A/A Two copies of the version the research linked to Hypothyroidism. 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 Hypothyroidism. That is a smaller link than two copies.
G/G No copy of the version the research linked to Hypothyroidism. This is the starting point the study compared everyone against.
Source

Questions about rs12593201

What is rs12593201?

rs12593201 is a single position in the genome, in or near the RASGRP1 gene. Published research associates it with hypothyroidism. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs12593201 linked to?

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

Does having rs12593201 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 rs12593201 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Hypothyroidism (rs12593201). MyGeneLog™. https://www.mygenelog.com/variants/rs12593201

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