| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1535724 | 1.000 | 0.120 | 13 | 75609137 | intron variant | G/C;T | snv | 1 | |||
| rs1711347 | 1.000 | 0.120 | 1 | 243998680 | intron variant | G/A | snv | 0.53 | 1 | ||
| rs17376456 | 1.000 | 0.120 | 5 | 94221997 | intron variant | A/G | snv | 8.7E-02 | 1 | ||
| rs17404956 | 1.000 | 0.120 | 5 | 166962488 | regulatory region variant | A/G | snv | 5.5E-02 | 1 | ||
| rs200903070 | 1.000 | 0.120 | 7 | 134448044 | missense variant | G/A | snv | 6.4E-05 | 1.1E-04 | 1 | |
| rs202069793 | 1.000 | 0.120 | 9 | 104713014 | intergenic variant | GA/- | delins | 0.63 | 1 | ||
| rs2031236 | 1.000 | 0.120 | 13 | 75595641 | intron variant | G/A;T | snv | 1 | |||
| rs2038823 | 1.000 | 0.120 | 13 | 96299179 | intron variant | G/A;T | snv | 1 | |||
| rs2055858 | 1.000 | 0.120 | 15 | 45022070 | upstream gene variant | G/C | snv | 0.19 | 1 | ||
| rs2070682 | 1.000 | 0.120 | 7 | 101133986 | intron variant | T/C | snv | 0.44 | 1 | ||
| rs2104455 | 1.000 | 0.120 | 6 | 9368285 | intergenic variant | A/G | snv | 0.30 | 1 | ||
| rs227453 | 1.000 | 0.120 | 6 | 165065309 | intron variant | A/T | snv | 0.18 | 1 | ||
| rs227455 | 1.000 | 0.120 | 6 | 165064562 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs2296146 | 1.000 | 0.120 | 13 | 75569436 | non coding transcript exon variant | T/A;C | snv | 4.5E-06; 0.18 | 1 | ||
| rs2300993 | 1.000 | 0.120 | 5 | 109702928 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs2328963 | 1.000 | 0.120 | 13 | 75601390 | intron variant | C/A;T | snv | 1 | |||
| rs2328964 | 1.000 | 0.120 | 13 | 75564694 | intron variant | G/T | snv | 0.79 | 1 | ||
| rs2811893 | 1.000 | 0.120 | 1 | 58696476 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs3007729 | 1.000 | 0.120 | 1 | 18468761 | regulatory region variant | T/C;G | snv | 1 | |||
| rs3783028 | 1.000 | 0.120 | 13 | 75591146 | intron variant | T/C | snv | 0.77 | 1 | ||
| rs3818355 | 1.000 | 0.120 | 13 | 75622731 | intron variant | C/T | snv | 0.80 | 1 | ||
| rs3844492 | 1.000 | 0.120 | 10 | 48614756 | intron variant | A/G | snv | 0.38 | 1 | ||
| rs39059 | 1.000 | 0.120 | 7 | 29215854 | intron variant | A/G | snv | 0.32 | 1 | ||
| rs4470583 | 1.000 | 0.120 | 4 | 161329780 | intergenic variant | A/G;T | snv | 1 | |||
| rs476141 | 1.000 | 0.120 | 1 | 244013122 | intron variant | G/A;T | snv | 1 |