| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2836411 | 1.000 | 0.040 | 21 | 38447907 | intron variant | C/A;T | snv | 1 | |||
| rs767169659 | 1.000 | 0.040 | 3 | 123733800 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs77294580 | 1.000 | 0.040 | 17 | 63480396 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs782591769 | 1.000 | 0.040 | 7 | 74045237 | missense variant | G/C | snv | 8.0E-06 | 1 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1419338705 | 1.000 | 0.040 | 7 | 74048163 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs766407419 | 1.000 | 0.040 | 17 | 1745008 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs2306691 | 1.000 | 0.040 | 12 | 57145019 | missense variant | A/G | snv | 2.0E-05 | 2.1E-05 | 1 | |
| rs121917864 | 0.645 | 0.520 | 4 | 153704936 | missense variant | C/T | snv | 8.8E-05 | 9.8E-05 | 31 | |
| rs3025058 | 0.658 | 0.600 | 11 | 102845217 | upstream gene variant | -/C;G | ins | 2.8E-04 | 26 | ||
| rs8125581 | 1.000 | 0.040 | 20 | 46010604 | missense variant | G/A | snv | 3.0E-04 | 3.4E-04 | 1 | |
| rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 98 | |
| rs595244 | 0.882 | 0.080 | 15 | 48548638 | intron variant | C/T | snv | 7.7E-02 | 3 | ||
| rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
| rs2276109 | 0.701 | 0.440 | 11 | 102875061 | upstream gene variant | T/C | snv | 9.2E-02 | 18 | ||
| rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 15 | ||
| rs3827066 | 0.925 | 0.040 | 20 | 45957384 | intron variant | C/T | snv | 0.12 | 2 | ||
| rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 68 | |
| rs58749629 | 1.000 | 0.040 | 20 | 45942678 | intron variant | G/A;T | snv | 0.13 | 1 | ||
| rs3918242 | 0.602 | 0.680 | 20 | 46007337 | upstream gene variant | C/T | snv | 0.14 | 54 | ||
| rs10985349 | 1.000 | 0.040 | 9 | 121662964 | intron variant | C/T | snv | 0.17 | 1 | ||
| rs6674171 | 1.000 | 0.040 | 1 | 154519207 | intron variant | A/G;T | snv | 0.19 | 1 | ||
| rs1057335 | 0.827 | 0.120 | 17 | 1754359 | missense variant | G/A | snv | 0.22 | 0.20 | 5 | |
| rs5186 | 0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 | 38 | |
| rs326118 | 0.925 | 0.080 | 5 | 7868430 | intron variant | T/G | snv | 0.21 | 2 |