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. 2018 Oct 12;9:4228. doi: 10.1038/s41467-018-06620-4

Table 2.

Exome-wide significant genes for serum urate in primary SKAT-O meta-analysis of low-frequency (MAF < 5%) putative damaging variants

Serum urate Gout
Race Number of variants SKAT-O P-Value Burden Beta Burden SE Burden P-Value SKAT P-Value Number of variants Burden OR Burden Beta Burden SE Burden P-Value
SLC22A12
EA and AA 97 1.3E-56 −0.033 0.002 6.7E-57 3.98E-19 60 0.50 −0.700 0.249 4.93E-03
 EA 78 5.1E-42 −0.033 0.002 2.5E-42 1.48E-18 48 0.41 −0.894 0.322 5.52E-03
 AA 27 6.4E-16 −0.035 0.004 3.2E-16 8.31E-10 15 0.66 −0.412 0.393 2.94E-01
SLC2A9
EA and AA 90 4.5E-07 −0.004 0.001 2.2E-03 2.27E-07 48 0.85 −0.157 0.116 1.73E-01
 EA 71 8.5E-07 −0.006 0.002 1.5E-04 4.25E-07 36 0.78 −0.249 0.142 7.92E-02
 AA 28 3.50E-02 −0.001 0.003 6.90E-01 2.00E-02 17 1.03 0.024 0.200 9.03E-01

Exome-wide significant p-value for SKAT-O = 1.28e-6 (= 0.05/19461 genes with 2 or more variants x2 primary SKAT-O tests)

Burden test for gout was conducted using uniform weight for estimating the effect per variant

SE standard error, EA European ancestry, AA African-American, OR odds ratio, SKAT-O optimal sequence kernel association test