| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35748167 | 1.000 | 0.120 | 18 | 60370200 | intron variant | G/C;T | snv | 1 | |||
| rs8113877 | 1.000 | 0.120 | 20 | 46006406 | upstream gene variant | G/T | snv | 0.55 | 1 | ||
| rs146850453 | 1.000 | 0.120 | 13 | 49630937 | missense variant | G/A;C | snv | 3.7E-04; 4.1E-06 | 1 | ||
| rs228014 | 1.000 | 0.120 | 1 | 177002472 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs369203092 | 1.000 | 0.120 | 11 | 108247117 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
| rs371713984 | 1.000 | 0.120 | 11 | 108247110 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs9288953 | 1.000 | 0.120 | 3 | 112484405 | intron variant | C/T | snv | 0.27 | 1 | ||
| rs567060474 | 1.000 | 0.120 | 11 | 108326070 | missense variant | G/A;T | snv | 1.0E-04 | 1 | ||
| rs2307842 | 1.000 | 0.120 | 12 | 103947867 | 3 prime UTR variant | GACT/-;GACTGACT | delins | 0.15 | 1 | ||
| rs2466032 | 1.000 | 0.120 | 8 | 127197575 | non coding transcript exon variant | T/C | snv | 0.23 | 1 | ||
| rs2266690 | 1.000 | 0.120 | 5 | 87399457 | missense variant | A/G;T | snv | 1 | |||
| rs3136687 | 1.000 | 0.120 | 17 | 40561644 | intron variant | T/C | snv | 0.18 | 1 | ||
| rs3805500 | 1.000 | 0.120 | 5 | 31462870 | intron variant | G/A | snv | 0.60 | 1 | ||
| rs2147420 | 1.000 | 0.120 | 10 | 88999856 | intron variant | A/G | snv | 0.50 | 1 | ||
| rs4505265 | 1.000 | 0.120 | 15 | 81185114 | intron variant | A/C | snv | 1 | |||
| rs1278359106 | 1.000 | 0.120 | 12 | 43777710 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs2705511 | 1.000 | 0.120 | 3 | 112460632 | downstream gene variant | A/C;G | snv | 1 | |||
| rs746910913 | 1.000 | 0.120 | 12 | 68839310 | frameshift variant | C/-;CC | delins | 1 | |||
| rs1057519832 | 1.000 | 0.120 | 16 | 81928578 | missense variant | A/C;G;T | snv | 1 | |||
| rs143635917 | 1.000 | 0.120 | 7 | 124842843 | missense variant | T/C | snv | 4.5E-04 | 4.1E-04 | 1 | |
| rs11688943 | 1.000 | 0.120 | 2 | 200875545 | intron variant | T/C | snv | 0.30 | 1 | ||
| rs1776948 | 1.000 | 0.120 | 20 | 4950467 | intron variant | G/A;C | snv | 1 | |||
| rs6133175 | 1.000 | 0.120 | 20 | 4911113 | intron variant | A/G | snv | 0.28 | 1 | ||
| rs17676986 | 1.000 | 0.120 | 7 | 127996905 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs1349826807 | 1.000 | 0.120 | 16 | 75648280 | missense variant | G/A | snv | 7.9E-05 | 4.2E-05 | 1 |