Table 1.
Trait | SNP | Chr1 | Position2 | Gene symbol3 | Tested allele | N | Ln Effect4 (95% CI) |
Effect in secs5 (95% CI) |
p-value6 |
---|---|---|---|---|---|---|---|---|---|
aPTT | rs2545801 | 5 | 176773945 | F12 | A | 2498 | 0.05 (0.04,0.06) |
1.05 (1.04,1.06) |
1.39×10−59 |
aPTT | rs1801020 | 5 | 176769138 | F12 | A | 2505 | 0.05 (0.05,0.06) |
1.05 (1.05,1.06) |
1.55×10−59 |
aPTT | rs17876032 | 5 | 176763233 | F12 | G | 2507 | 0.04 (0.03,0.04) |
1.04 (1.03,1.04) |
1.40×10−37 |
aPTT | rs710446 | 3 | 187942621 | KNG1 | G | 2501 | −0.03 (−0.03,−0.02) |
0.97 (0.97,0.98) |
2.68×10−19 |
aPTT | rs2228243 | 3 | 187877807 | HRG | G | 2503 | 0.03 (0.02,0.04) |
1.03 (1.02,1.04) |
1.35×10−17 |
aPTT | rs16860992 | 3 | 187876732 | HRG | C | 2503 | 0.03 (0.02,0.04) |
1.03 (1.02,1.04) |
4.37×10−17 |
aPTT | rs5030062 | 3 | 187936874 | KNG1 | C | 2506 | −0.02 (−0.03,−0.02) |
0.98 (0.97,0.98) |
3.55×10−15 |
aPTT | rs1621816 | 3 | 187921867 | KNG1 | G | 2500 | 0.02 (0.02,0.03) |
1.02 (1.02,1.03) |
2.33×10−14 |
aPTT | rs5030028 | 3 | 187928448 | KNG1 | A | 2502 | 0.03 (0.02,0.03) |
1.03 (1.02,1.03) |
3.78×10−14 |
aPTT | rs5030023 | 3 | 187927338 | KNG1 | A | 2508 | 0.03 (0.02,0.03) |
1.03 (1.02,1.03) |
4.16×10−14 |
aPTT | rs3856930 | 3 | 187941016 | KNG1 | A | 2506 | −0.02 (−0.03,−0.02) |
0.98 (0.97,0.98) |
6.90×10−14 |
aPTT | rs1624230 | 3 | 187921629 | KNG1 | A | 2499 | 0.02 (0.02,0.03) |
1.02 (1.02,1.03) |
9.47×10−14 |
aPTT | rs657152 | 9 | 135129086 | ABO | A | 2507 | −0.02 (−0.03,−0.01) |
0.98 (0.97,0.99) |
2.45×10−11 |
aPTT | rs266723 | 3 | 187929741 | KNG1 | C | 2501 | 0.02 (0.01,0.02) |
1.02 (1.01,1.02) |
3.31×10−10 |
aPTT | rs7447593 | 5 | 176756743 | F12 | C | 2504 | −0.02 (−0.02,−0.01) |
0.98 (0.98,0.99) |
1.81×10−09 |
aPTT | rs7381103 | 5 | 176770918 | F12 | G | 2510 | 0.05 (0.03,0.07) |
1.05 (1.03,1.07) |
4.35×10−09 |
aPTT | rs651007 | 9 | 135143696 | ABO | A | 2502 | −0.02 (−0.03,−0.01) |
0.98 (0.97,0.99) |
5.97×10−09 |
aPTT | rs1042445 | 3 | 187878130 | HRG | A | 2508 | −0.02 (−0.03,−0.01) |
0.98 (0.97,0.99) |
2.27×10−08 |
aPTT | rs1624569 | 3 | 187932763 | KNG1 | G | 2499 | 0.02 (0.01,0.02) |
1.02 (1.01,1.02) |
5.15×10−08 |
aPTT | rs2062632 | 3 | 187943875 | KNG1 | G | 2503 | 0.02 (0.01,0.02) |
1.02 (1.01,1.02) |
1.04×10−07 |
aPTT | rs2287694 | 5 | 176792899 | GRK6 | G | 2508 | 0.02 (0.02,0.03) |
1.02 (1.02,1.03) |
1.39×10−07 |
aPTT | rs4253304 | 4 | 187410565 | KLKB1 | C | 2498 | −0.01 (−0.02,−0.01) |
0.99 (0.98,0.99) |
1.67×10−07 |
aPTT | rs13177732 | 5 | 176789531 | GRK6 | C | 2500 | −0.02 (−0.02,−0.01) |
0.98 (0.98,0.99) |
2.56×10−07 |
aPTT | rs9898 | 3 | 187873321 | HRG | A | 2505 | 0.02 (0.01,0.02) |
1.02 (1.01,1.02) |
2.61×10−07 |
aPTT | rs2304595 | 4 | 187409274 | KLKB1 | A | 2507 | −0.01 (−0.02,−0.01) |
0.99 (0.98,0.99) |
3.60×10−07 |
aPTT | rs5030091 | 3 | 187943571 | KNG1 | G | 2507 | 0.01 (0.01,0.02) |
1.01 (1.01,1.02) |
7.29×10−07 |
APC-R | rs6025 | 1 | 1.68E+08 | F5 | A | 2500 | −0.28 (−0.31,−0.26) |
0.76 (0.73,0.77) |
4.2×10−104 |
APC-R | rs6682179 | 1 | 1.68E+08 | F5 | A | 2499 | −0.08 (−0.1,−0.07) |
0.92 (0.9,1.07) |
1.43×10−28 |
APC-R | rs6427196 | 1 | 1.68E+08 | F5 | C | 2500 | −0.08 (−0.1,−0.07) |
0.92 (0.9,1.07) |
2.11×10−28 |
APC-R | rs6009 | 1 | 1.68E+08 | F5 | A | 2500 | −0.08 (−0.1,−0.07) |
0.92 (0.9,1.07) |
1.24×10−27 |
APC-R | rs16860992 | 3 | 1.88E+08 | HRG | C | 2492 | 0.04 (0.03,0.04) |
1.04 (1.03,1.04) |
2.29×10−15 |
APC-R | rs2228243 | 3 | 1.88E+08 | HRG | G | 2492 | 0.03 (0.03,0.04) |
1.03 (1.03,1.04) |
9.55×10−15 |
APC-R | rs9898 | 3 | 1.88E+08 | HRG | A | 2496 | 0.02 (0.02,0.03) |
1.02 (1.02,1.03) |
5.26×10−11 |
APC-R | rs2038024 | 1 | 1.68E+08 | SLC19A2 | C | 2496 | −0.03 (−0.04,−0.02) |
0.97 (0.96,0.98) |
1.75×10−09 |
Both aPTT and APC resistance (“traits”) are presented in this table.
Chromosome (“Chr”).
Chromosomal position.
Mapped gene.
Logged effect sizes (as tested by regression).
Anti-logged effect sizes (for direct interpretation), where effect is change in trait per tested allele.
P-value indicates strength of evidence against the null hypothesis as tested by linear regression of trait on number of tested alleles.