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Who was studied 41,917 European ancestry bipolar disorder cases, 12,366 European ancestry ulcerative colitis cases, 405,158 European ancestry controls.
The effect
Each copy of the T allele shifted the measure 0.016 lower (95% confidence interval 0.012-0.02); p = 3 × 10−13.
Where it sits Chromosome 12, band 12p13.33 — in an intron of CACNA1C.
What each result means
C/CNo copy of the version the research linked to Bipolar disorder or ulcerative colitis (MTAG). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Bipolar disorder or ulcerative colitis (MTAG). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Bipolar disorder or ulcerative colitis (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
Journal of affective disorders · 2024 · PMID 38154582
Questions about rs2238056
What is rs2238056?
rs2238056 is a single position in the genome, in or near the CACNA1C gene. Published research associates it with bipolar disorder or ulcerative colitis (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs2238056 linked to?
On MyGeneLog this position is linked to Ulcerative Colitis. The research behind each link, and its sources, are set out on that condition page.
Does having rs2238056 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 rs2238056 come from?
GWAS Catalog, Journal of affective disorders 2024, PMID:38154582. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Bipolar disorder or ulcerative colitis (MTAG) (rs2238056). MyGeneLog™. https://www.mygenelog.com/variants/rs2238056