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Who was studied 29,739 Japanese ancestry cases, 240,675 Japanese ancestry controls.
The effect
Each copy of the A allele shifted the measure 0.148 higher (95% confidence interval 0.11-0.18); p = 4 × 10−15.
How common The A allele had a frequency of about 10% in the people studied.
Where it sits Chromosome 7, band 7q32.1 — in an intron of SND1.
What each result means
A/ATwo copies of the version the research linked to Peptic ulcer disease. 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 Peptic ulcer disease. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Peptic ulcer disease. This is the starting point the study compared everyone against.
Nature genetics · 2023 · PMID 38036781 · open access
Questions about rs72607744
What is rs72607744?
rs72607744 is a single position in the genome, in or near the SND1 gene. Published research associates it with peptic ulcer 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 rs72607744 linked to?
On MyGeneLog this position is linked to Peptic Ulcer Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs72607744 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 rs72607744 come from?
GWAS Catalog, Nature genetics 2023, PMID:38036781. 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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