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Who was studied 23,553 European ancestry individuals, 23,536 Japanese individuals, 16,325 Hispanic individuals, 8,224 African American individuals.
The effect
Each copy of the T allele shifted the measure 0.897 lower (95% confidence interval 0.55-1.25); p = 6 × 10−7.
How common The T allele had a frequency of about 30% in the people studied.
Where it sits Chromosome 5, band 5q35.3 — in a regulatory region of SLC34A1.
What each result means
C/CNo copy of the version the research linked to Glomerular filtration rate. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Glomerular filtration rate. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Glomerular filtration rate. That is the strongest link of the three results. A link in a study is not a diagnosis.
American journal of human genetics · 2016 · PMID 27588450 · open access
Questions about rs35716097
What is rs35716097?
rs35716097 is a single position in the genome, in or near the SLC34A1 gene. Published research associates it with glomerular filtration rate. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs35716097 linked to?
On MyGeneLog this position is linked to Kidney Function. The research behind each link, and its sources, are set out on that condition page.
Does having rs35716097 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 rs35716097 come from?
GWAS Catalog, Am J Hum Genet 2016, PMID:27588450. 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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