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. 2006 Oct 18;121(1):23–34. doi: 10.1007/s00439-006-0260-8

Table 1.

Genes with significant association with warfarin dose, based on univariate regression of square root of dose

Gene SNP MAF n Univariate R2 P-Value r2 with best SNP
VKORC1 rs9923231 0.391 181 0.317 1.91 × 10−15**
rs2359612 0.389 200 0.290 2.30 × 10−15** 0.968
rs9934438 0.383 169 0.292 3.59 × 10−13** 1.000
rs7294 0.384 188 0.208 4.14 × 10−10** 0.385
rs4889490 0.446 199 0.160 3.821 × 10−8** 0.461
rs4889537 0.372 199 0.142 3.158 × 10−7** 0.209
rs4889599 0.366 194 0.124 3.270 × 10−6** 0.305
rs8046978 0.214 197 0.047 0.00906 0.173
rs11642603 0.093 192 0.027 0.02304 0.070
rs11642466 0.103 195 0.025 0.02623 0.080
rs7194347 0.343 197 0.032 0.04069 0.153
CYP2C9 rs1057910 (*3) 0.058 201 0.141 2.784 × 10−7**
rs9332108 0.064 201 0.141 2.784 × 10−7** 0.890
rs9325473 0.055 189 0.147 3.753 × 10−7** 0.908
rs1057911 0.067 191 0.145 4.218 × 10−7** 0.890
rs9332214 0.059 198 0.139 4.654 × 10−7** 0.878
rs4917639 0.173 197 0.118 4.944 × 10−6** 0.276
rs2860905 0.214 193 0.072 0.00080* 0.224
CYP2C19 rs3814637 0.059 195 0.106 0.00002** 0.838a
rs17882687(*15) 0.08 183 0.044 0.00417* 0.395a
CYP2C18 rs7896133 0.056 193 0.074 0.00013** 0.869a
PROC rs2069919 0.372 182 0.090 0.00022*
rs1799809 0.433 188 0.078 0.00055* 0.777
rs2069901 0.441 177 0.072 0.00147* 0.785
rs2069910 0.387 178 0.046 0.01678 0.414
APOE rs429358 + rs7412b 0.251 201 0.051 0.00570*
EPHX1 rs4653436 0.266 196 0.048 0.00848
CALU rs11653 0.366 197 0.047 0.00944
rs1006023 0.331 200 0.033 0.03789 0.865
rs2307040 0.336 200 0.033 0.03811 0.867
rs339054 0.461 195 0.032 0.04487 0.612
GGCX rs12714145 0.408 198 0.034 0.03320
ORM1-2 rs1687390 0.062 149 0.026 0.04964

The SNPs are listed with the lowest P-value first. The LD (r2) between the SNP with the lowest P-value and others in the gene or gene cluster is shown. n is the number of successfully genotyped individuals

aLinkage disequilibrium with CYP2C9*3 (rs10579103)

bNote that the two APOE SNPs are not significant individually, only when assessed as E2 + E4 vs. E3

*The test is significant, based on correction for the effective number of tests in each gene or gene cluster

**Corresponds to experiment-wise significance, based on ∼285 independent effective tests (P < 1.75 × 10−4)