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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 2,216 European ancestry cases, 5,594 Europen ancestry controls.
The effect
Each copy of the C allele carried 3.71 times the odds of Primary biliary cirrhosis (95% confidence interval 3.00-4.59); p = 1 × 10−33.
Where it sits Chromosome 6, band 6p21.32 — between genes, 16 kb from MTCO3P1.
What each result means
C/CTwo copies of the version the research linked to Primary biliary cirrhosis. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Primary biliary cirrhosis. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Primary biliary cirrhosis. This is the starting point the study compared everyone against.
rs7775055 is a single position in the genome, in or near the near MTCO3P1 gene. Published research associates it with primary biliary cirrhosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7775055 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 rs7775055 come from?
GWAS Catalog, Human molecular genetics 2012, PMID:22936693. 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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