| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10019658 | 1.000 | 0.040 | 4 | 34423326 | intergenic variant | A/G | snv | 0.22 | 1 | ||
| rs1008878 | 1.000 | 0.040 | 9 | 22036113 | non coding transcript exon variant | G/T | snv | 0.71 | 2 | ||
| rs1010053 | 0.925 | 0.080 | 14 | 60538907 | intron variant | A/G | snv | 0.34 | 2 | ||
| rs10106029 | 1.000 | 0.040 | 8 | 104969975 | intron variant | A/G | snv | 0.59 | 1 | ||
| rs10115049 | 1.000 | 0.040 | 9 | 22032120 | intron variant | A/G | snv | 0.46 | 2 | ||
| rs10116277 | 0.827 | 0.160 | 9 | 22081398 | intron variant | G/T | snv | 0.62 | 8 | ||
| rs10120688 | 0.807 | 0.080 | 9 | 22056500 | intron variant | G/A | snv | 0.50 | 7 | ||
| rs10120806 | 1.000 | 0.040 | 9 | 22047946 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs1015213 | 0.851 | 0.040 | 8 | 51974981 | intron variant | C/T | snv | 0.14 | 6 | ||
| rs1018533 | 1.000 | 0.040 | 14 | 60504419 | intron variant | T/C | snv | 0.63 | 1 | ||
| rs10483727 | 0.851 | 0.040 | 14 | 60606157 | upstream gene variant | T/C | snv | 0.45 | 4 | ||
| rs1048661 | 0.732 | 0.320 | 15 | 73927205 | missense variant | G/T | snv | 0.33 | 0.28 | 14 | |
| rs1052990 | 0.882 | 0.040 | 7 | 116508316 | 3 prime UTR variant | T/C;G | snv | 3 | |||
| rs1063192 | 0.695 | 0.520 | 9 | 22003368 | 3 prime UTR variant | G/A;T | snv | 24 | |||
| rs10738604 | 1.000 | 0.040 | 9 | 22025494 | intron variant | G/A | snv | 0.29 | 3 | ||
| rs10738605 | 0.925 | 0.120 | 9 | 22049131 | non coding transcript exon variant | C/A;G | snv | 3 | |||
| rs10757263 | 1.000 | 0.040 | 9 | 22013806 | non coding transcript exon variant | C/T | snv | 0.56 | 1 | ||
| rs10757265 | 1.000 | 0.040 | 9 | 22048860 | intron variant | T/C | snv | 0.49 | 2 | ||
| rs10757266 | 1.000 | 0.040 | 9 | 22049556 | intron variant | C/G;T | snv | 1 | |||
| rs10757267 | 1.000 | 0.040 | 9 | 22052811 | intron variant | G/A;C;T | snv | 2 | |||
| rs10757269 | 1.000 | 0.040 | 9 | 22072265 | intron variant | A/C;G | snv | 4 | |||
| rs10757270 | 1.000 | 0.040 | 9 | 22072720 | intron variant | A/C;G | snv | 0.40 | 2 | ||
| rs10811640 | 1.000 | 0.040 | 9 | 22013412 | non coding transcript exon variant | G/T | snv | 0.56 | 1 | ||
| rs10811641 | 1.000 | 0.040 | 9 | 22014138 | non coding transcript exon variant | C/G | snv | 0.32 | 2 | ||
| rs10811643 | 1.000 | 0.040 | 9 | 22024967 | intron variant | A/G | snv | 0.56 | 2 |