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Its strongest genetic-study result is p = 10−19, with 1 associations in the GWAS Catalog.
How this is scored
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 6,223 European ancestry cases, 482,123 European ancestry controls, 11,699 East Asian ancestry cases, 167,027 East Asian ancestry controls.
The effect
Each copy of the G allele shifted the measure 0.12 higher (95% confidence interval 0.094-0.146); p = 6 × 10−20.
Where it sits Chromosome 1, band 1p36.12 — between genes, 5.2 kb from ALPL.
What each result means
G/GTwo copies of the version the research linked to Urolithiasis. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to Urolithiasis. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Urolithiasis. This is the starting point the study compared everyone against.
rs13353032 is a single position in the genome, in or near the near ALPL gene. Published research associates it with urolithiasis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs13353032 linked to?
On MyGeneLog this position is linked to Urolithiasis. The research behind each link, and its sources, are set out on that condition page.
Does having rs13353032 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 rs13353032 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.
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Quoting this page
Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license