Abstract
Using genome-wide association, we identify common variants at 2p12-p13, 6q26, 17q23 and 19q13 associated with serum creatinine, a marker of kidney function (P = 10(-10) to 10(-15)). Of these, rs10206899 (near NAT8, 2p12-p13) and rs4805834 (near SLC7A9, 19q13) were also associated with chronic kidney disease (P = 5.0 x 10(-5) and P = 3.6 x 10(-4), respectively). Our findings provide insight into metabolic, solute and drug-transport pathways underlying susceptibility to chronic kidney disease.
| Original language | English |
|---|---|
| Pages (from-to) | 373-375 |
| Number of pages | 3 |
| Journal | Nature Genetics |
| Volume | 42 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - May-2010 |
Keywords
- OCT2
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