| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1064395 | 0.882 | 0.120 | 19 | 19250926 | 3 prime UTR variant | G/A | snv | 0.24 | 1 | ||
| rs10744560 | 0.882 | 0.040 | 12 | 2277933 | intron variant | C/G;T | snv | 3 | |||
| rs10745843 | 0.925 | 0.040 | 12 | 99102252 | intron variant | G/A | snv | 0.55 | 2 | ||
| rs10748045 | 0.925 | 0.040 | 12 | 66422359 | intron variant | A/G | snv | 0.41 | 3 | ||
| rs10761473 | 1.000 | 0.040 | 10 | 60300624 | intron variant | C/G | snv | 0.12 | 1 | ||
| rs10774035 | 0.925 | 0.040 | 12 | 2259508 | intron variant | C/A;T | snv | 1 | |||
| rs10774037 | 0.882 | 0.040 | 12 | 2311360 | intron variant | G/A | snv | 0.77 | 3 | ||
| rs10821736 | 1.000 | 0.040 | 10 | 60345295 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs10821745 | 1.000 | 0.040 | 10 | 60376448 | intron variant | T/G | snv | 9.7E-02 | 1 | ||
| rs10821748 | 1.000 | 0.040 | 10 | 60393180 | intron variant | G/C | snv | 0.12 | 1 | ||
| rs10821789 | 1.000 | 0.040 | 10 | 60525580 | intron variant | G/A | snv | 9.2E-02 | 1 | ||
| rs10821792 | 1.000 | 0.040 | 10 | 60538858 | intron variant | C/T | snv | 8.3E-02 | 1 | ||
| rs10848642 | 1.000 | 0.040 | 12 | 2222406 | non coding transcript exon variant | A/G | snv | 0.37 | 1 | ||
| rs10858583 | 1.000 | 0.040 | 12 | 87334666 | intergenic variant | C/T | snv | 0.79 | 3 | ||
| rs10865974 | 0.925 | 0.040 | 3 | 52684264 | intron variant | G/C;T | snv | 2 | |||
| rs10875914 | 1.000 | 0.040 | 12 | 49028311 | intron variant | A/G | snv | 0.44 | 2 | ||
| rs10878840 | 1.000 | 0.040 | 12 | 68487269 | upstream gene variant | G/A | snv | 0.62 | 1 | ||
| rs10884920 | 1.000 | 0.040 | 10 | 110015049 | intron variant | A/G;T | snv | 1 | |||
| rs10889182 | 1.000 | 0.040 | 1 | 60532523 | intron variant | T/G | snv | 0.33 | 1 | ||
| rs10889187 | 1.000 | 0.040 | 1 | 60545086 | intron variant | G/A | snv | 0.33 | 1 | ||
| rs10889189 | 1.000 | 0.040 | 1 | 60559354 | intron variant | C/G | snv | 0.47 | 1 | ||
| rs10896090 | 1.000 | 0.040 | 11 | 66177715 | intron variant | A/G | snv | 0.16 | 1 | ||
| rs10896135 | 1.000 | 0.040 | 11 | 66783531 | intron variant | G/A;C | snv | 1 | |||
| rs10968749 | 0.851 | 0.040 | 9 | 28752486 | intergenic variant | A/G | snv | 5.5E-02 | 4 | ||
| rs10994299 | 1.000 | 0.040 | 10 | 60316870 | intron variant | C/A | snv | 6.8E-02 | 1 |