| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10004892 | 1.000 | 0.040 | 4 | 188951696 | intergenic variant | T/C | snv | 0.21 | 1 | ||
| rs10006108 | 1.000 | 0.040 | 4 | 97002862 | intergenic variant | C/T | snv | 0.48 | 1 | ||
| rs10019259 | 1.000 | 0.040 | 4 | 95825984 | intergenic variant | C/A;T | snv | 1 | |||
| rs10027671 | 1.000 | 0.040 | 4 | 153056676 | intron variant | G/A | snv | 0.35 | 1 | ||
| rs10029800 | 1.000 | 0.040 | 4 | 152071589 | intergenic variant | C/A | snv | 0.63 | 1 | ||
| rs10039512 | 1.000 | 0.040 | 5 | 68847366 | intron variant | C/G;T | snv | 1 | |||
| rs10040260 | 1.000 | 0.040 | 5 | 1749100 | intergenic variant | C/A;G | snv | 1 | |||
| rs10041756 | 1.000 | 0.040 | 5 | 22996131 | intergenic variant | G/A | snv | 0.14 | 1 | ||
| rs10052628 | 1.000 | 0.040 | 5 | 25949752 | intergenic variant | C/T | snv | 7.8E-02 | 1 | ||
| rs10053503 | 1.000 | 0.040 | 5 | 104778862 | intron variant | T/G | snv | 8.3E-02 | 1 | ||
| rs10053765 | 1.000 | 0.040 | 5 | 99658228 | intergenic variant | T/C | snv | 0.49 | 1 | ||
| rs10064843 | 1.000 | 0.040 | 5 | 25948342 | regulatory region variant | G/A | snv | 0.17 | 1 | ||
| rs10067455 | 1.000 | 0.040 | 5 | 88162105 | intergenic variant | G/T | snv | 0.82 | 1 | ||
| rs10069142 | 1.000 | 0.040 | 5 | 115777468 | upstream gene variant | A/G;T | snv | 1 | |||
| rs1007126 | 1.000 | 0.040 | 20 | 51252774 | intergenic variant | A/G | snv | 0.34 | 1 | ||
| rs10071650 | 1.000 | 0.040 | 5 | 29900854 | intergenic variant | T/A;C | snv | 1 | |||
| rs10076002 | 1.000 | 0.040 | 5 | 68858473 | intron variant | G/A | snv | 0.61 | 1 | ||
| rs10078652 | 1.000 | 0.040 | 5 | 104781996 | intron variant | T/C | snv | 0.29 | 1 | ||
| rs10079889 | 1.000 | 0.040 | 5 | 32975384 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs10084407 | 1.000 | 0.040 | 2 | 204453777 | regulatory region variant | C/A | snv | 0.15 | 1 | ||
| rs10084416 | 1.000 | 0.040 | 2 | 204453879 | regulatory region variant | G/C | snv | 0.32 | 1 | ||
| rs1008532 | 1.000 | 0.040 | 20 | 55893002 | regulatory region variant | C/T | snv | 9.6E-02 | 1 | ||
| rs10086987 | 1.000 | 0.040 | 8 | 47177908 | intron variant | G/A;C | snv | 1 | |||
| rs10092798 | 1.000 | 0.040 | 8 | 135744067 | upstream gene variant | T/C | snv | 0.15 | 1 | ||
| rs10092799 | 1.000 | 0.040 | 8 | 13757626 | intergenic variant | A/C | snv | 8.3E-02 | 1 |