| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 5 | |||
| rs5030809 | 0.776 | 0.320 | 3 | 10142139 | missense variant | T/C | snv | 1.3E-05 | 2 | ||
| rs5030820 | 0.827 | 0.280 | 3 | 10149822 | missense variant | C/G;T | snv | 8.0E-06 | 2 | ||
| rs5030821 | 0.827 | 0.280 | 3 | 10149823 | missense variant | G/A;C;T | snv | 4.0E-06 | 2 | ||
| rs587782274 | 1.000 | 0.120 | 11 | 108312465 | missense variant | A/C | snv | 1 | |||
| rs876658517 | 1.000 | 0.120 | 11 | 108327735 | missense variant | A/G;T | snv | 1 | |||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
| rs1397145500 | 1.000 | 0.120 | 17 | 64066782 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs78683075 | 1.000 | 0.120 | 17 | 17222565 | missense variant | G/A | snv | 2.6E-04 | 2.4E-04 | 1 | |
| rs372947534 | 1.000 | 0.120 | 5 | 180626237 | missense variant | G/A | snv | 4.0E-05 | 6.3E-05 | 1 | |
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
| rs149617956 | 0.672 | 0.560 | 3 | 69964940 | missense variant | G/A | snv | 1.4E-03 | 1.6E-03 | 1 | |
| rs121913250 | 0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv | 1 | |||
| rs147608663 | 1.000 | 0.120 | 5 | 97171338 | missense variant | A/G | snv | 2.8E-05; 8.1E-06 | 4.9E-05 | 1 | |
| rs104893824 | 0.776 | 0.320 | 3 | 10142181 | missense variant | T/A;C | snv | 1 | |||
| rs104893829 | 0.882 | 0.240 | 3 | 10142088 | missense variant | C/T | snv | 2.0E-04 | 3.8E-04 | 1 | |
| rs1064794272 | 0.807 | 0.240 | 3 | 10146566 | missense variant | C/A | snv | 1 | |||
| rs28940297 | 0.882 | 0.240 | 3 | 10149811 | missense variant | T/C;G | snv | 1 | |||
| rs397516440 | 0.851 | 0.280 | 3 | 10142166 | missense variant | C/G;T | snv | 4.5E-06 | 1 |