Table 2.

Association results for albuminuria in European Americans from the CKDGen Consortium

SNP ID	Nearest gene	Coded allele	Minor allele frequency	Directionality of the GFR related to the coded allele	Odds ratio related to the coded allele (95% confidence interval)	P-value*
rs17319721	SHROOM3	A	0.43	–	0.88 (0.83–0.93)	1.87E-06
rs11959928	DAB2	A	0.44	–	0.97 (0.92–1.02)	0.26
rs1394125	UBE2Q2	A	0.35	–	0.95 (0.90–1.01)	0.13
rs10109414	STC1	T	0.42	–	0.95 (0.91–1.00)	0.07
rs1260326	GCKR	T	0.41	+	1.07 (1.01–1.12)	0.02
rs267734	ANXA9	C	0.2	+	1.03 (0.97–1.10)	0.36
rs7805747	PRKAG2	A	0.24	–	1.07 (0.98–1.16)	0.15
rs4744712	PIP5K1B	A	0.39	–	0.96 (0.91–1.01)	0.11
rs6420094	SLC34A1	G	0.34	–	1.01 (0.94–1.08)	0.84
rs626277	DACH1	C	0.4	+	1.00 (0.95–1.06)	0.93
rs12460876	SLC7A9	C	0.39	+	0.97 (0.92–1.03)	0.30
rs653178	ATXN2	C	0.5	–	1.00 (0.94–1.05)	0.88
rs881858	VEGFA	G	0.28	+	1.00 (0.94–1.06)	0.95
rs13538	ALMS1	G	0.23	+	1.08 (1.02–1.16)	0.01
rs12917707	UMOD	T	0.18	+	1.03 (0.96–1.10)	0.46
rs347685	TFDP2	C	0.28	+	1.01 (0.95–1.07)	0.74

Statistical significance defined using a Bonferroni correction for the 16 SNPs (0.05/16 = 0.003).