Genetic loci influencing kidney function and chronic kidney disease in man
Chronic kidney disease (CKD), the result of permanent loss of kidney function, is a major global problem. We identify common genetic variants at chr2p12-p13, chr6q26, chr17q23 and chr19q13 associated with serum creatinine, a marker of kidney function (P=10 −10 to 10 −15 ). SNPs rs10206899 (near NAT8...
Saved in:
Published in | Nature genetics Vol. 42; no. 5; pp. 373 - 375 |
---|---|
Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
11.04.2010
|
Online Access | Get full text |
Cover
Loading…
Summary: | Chronic kidney disease (CKD), the result of permanent loss of kidney function, is a major global problem. We identify common genetic variants at chr2p12-p13, chr6q26, chr17q23 and chr19q13 associated with serum creatinine, a marker of kidney function (P=10
−10
to 10
−15
). SNPs rs10206899 (near
NAT8
, chr2p12-p13) and rs4805834 (near
SLC7A9
, chr19q13) were also associated with CKD. Our findings provide new insight into metabolic, solute and drug-transport pathways underlying susceptibility to CKD. |
---|---|
Bibliography: | These authors contributed equally to the work. |
ISSN: | 1061-4036 1546-1718 |
DOI: | 10.1038/ng.566 |