| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10020288 | 1.000 | 0.040 | 4 | 28686220 | intergenic variant | G/A | snv | 0.38 | 2 | ||
| rs1002656 | 1.000 | 0.040 | 1 | 36727140 | intergenic variant | C/T | snv | 0.56 | 1 | ||
| rs10035449 | 1.000 | 0.040 | 5 | 165059061 | intron variant | T/A;C | snv | 1 | |||
| rs10061069 | 1.000 | 0.040 | 5 | 93735924 | 3 prime UTR variant | G/C | snv | 0.28 | 1 | ||
| rs10065906 | 1.000 | 0.040 | 5 | 159580770 | intron variant | C/A | snv | 0.74 | 1 | ||
| rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
| rs1008042 | 1.000 | 0.040 | 10 | 4583381 | intergenic variant | C/A;T | snv | 1 | |||
| rs1011633 | 1.000 | 0.040 | 2 | 99478337 | intron variant | C/T | snv | 0.43 | 1 | ||
| rs10127497 | 1.000 | 0.040 | 1 | 66584461 | intron variant | A/T | snv | 0.19 | 1 | ||
| rs10144845 | 1.000 | 0.040 | 14 | 74771067 | intron variant | C/T | snv | 0.62 | 2 | ||
| rs10148293 | 1.000 | 0.040 | 14 | 74830128 | intron variant | A/G;T | snv | 0.48 | 1 | ||
| rs10149470 | 1.000 | 0.040 | 14 | 103551616 | upstream gene variant | A/G | snv | 0.54 | 3 | ||
| rs1014969 | 1.000 | 0.040 | 3 | 52774325 | upstream gene variant | G/A | snv | 0.44 | 1 | ||
| rs10156548 | 1.000 | 0.040 | 9 | 23318435 | intron variant | G/C;T | snv | 2 | |||
| rs10175979 | 1.000 | 0.040 | 2 | 57586038 | intergenic variant | C/G;T | snv | 1 | |||
| rs10198241 | 0.925 | 0.080 | 2 | 226115660 | intergenic variant | T/C | snv | 0.58 | 4 | ||
| rs1021363 | 1.000 | 0.040 | 10 | 104851081 | intron variant | A/G | snv | 0.74 | 1 | ||
| rs10233018 | 0.925 | 0.040 | 7 | 117883655 | non coding transcript exon variant | A/G | snv | 0.53 | 2 | ||
| rs10243383 | 1.000 | 0.040 | 7 | 22242733 | intron variant | C/T | snv | 0.51 | 2 | ||
| rs10274968 | 1.000 | 0.040 | 7 | 38899654 | intron variant | C/T | snv | 0.65 | 1 | ||
| rs1039197 | 1.000 | 0.040 | 10 | 4617005 | intergenic variant | A/C | snv | 0.71 | 1 | ||
| rs10405382 | 1.000 | 0.040 | 19 | 32405810 | 5 prime UTR variant | C/G | snv | 0.18 | 2 | ||
| rs10405744 | 0.851 | 0.040 | 19 | 19948684 | intron variant | G/A | snv | 9.0E-02 | 4 | ||
| rs1042779 | 0.882 | 0.040 | 3 | 52786995 | missense variant | A/G | snv | 0.40 | 0.42 | 3 | |
| rs10429537 | 1.000 | 0.040 | 9 | 23346844 | intron variant | C/G | snv | 0.33 | 2 |