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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 234 European ancestry cases, 5,606 European ancestry controls.
The effect
Each copy of the A allele carried 0.03 times the odds of Mastocytosis (95% confidence interval -1.93819-1.98965); p = 1 × 10−9.
How common The A allele had a frequency of about 8% in the people studied.
Where it sits Chromosome 21, band 21q22.3 — a missense change in FTCD.
What each result means
A/ATwo copies of the version the research linked to Mastocytosis. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Mastocytosis. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Mastocytosis. This is the starting point the study compared everyone against.
International journal of molecular sciences · 2020 · PMID 32752121 · open access
Questions about rs61735841
What is rs61735841?
rs61735841 is a single position in the genome, in or near the FTCD gene. Published research associates it with mastocytosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs61735841 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 rs61735841 come from?
GWAS Catalog, International journal of molecular sciences 2020, PMID:32752121. 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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