| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11603020 | 0.925 | 0.120 | 11 | 57606859 | intron variant | T/C | snv | 0.21 | 1 | ||
| rs2280141 | 1.000 | 0.040 | 10 | 122433665 | 3 prime UTR variant | T/G | snv | 0.56 | 3 | ||
| rs6585827 | 1.000 | 0.040 | 10 | 122406099 | intron variant | G/A | snv | 0.47 | 3 | ||
| rs10510110 | 0.925 | 0.120 | 10 | 122432914 | 3 prime UTR variant | T/C | snv | 0.56 | 2 | ||
| rs2421016 | 0.925 | 0.120 | 10 | 122407996 | intron variant | C/T | snv | 0.46 | 2 | ||
| rs1045216 | 1.000 | 0.040 | 10 | 122429681 | missense variant | A/G | snv | 0.68 | 0.69 | 1 | |
| rs10490924 | 0.716 | 0.240 | 10 | 122454932 | missense variant | G/T | snv | 0.26 | 0.23 | 1 | |
| rs10510109 | 1.000 | 0.040 | 10 | 122360941 | intergenic variant | G/A;T | snv | 1 | |||
| rs10749466 | 1.000 | 0.040 | 10 | 122379288 | intron variant | A/G | snv | 0.32 | 1 | ||
| rs10788284 | 1.000 | 0.040 | 10 | 122390401 | intron variant | T/C | snv | 0.55 | 1 | ||
| rs10887142 | 1.000 | 0.040 | 10 | 122347969 | downstream gene variant | G/A;C | snv | 1 | |||
| rs10887149 | 1.000 | 0.040 | 10 | 122407488 | intron variant | G/A;C | snv | 1 | |||
| rs10887150 | 1.000 | 0.040 | 10 | 122421062 | non coding transcript exon variant | C/A | snv | 0.47 | 1 | ||
| rs10887151 | 1.000 | 0.040 | 10 | 122421250 | non coding transcript exon variant | C/T | snv | 0.45 | 1 | ||
| rs11200576 | 1.000 | 0.040 | 10 | 122358034 | intergenic variant | A/T | snv | 0.13 | 1 | ||
| rs11200583 | 1.000 | 0.040 | 10 | 122363954 | regulatory region variant | A/C | snv | 0.13 | 1 | ||
| rs11200594 | 1.000 | 0.040 | 10 | 122379877 | intron variant | C/T | snv | 0.47 | 1 | ||
| rs11200595 | 1.000 | 0.040 | 10 | 122383113 | intron variant | T/A;C | snv | 1 | |||
| rs11200604 | 1.000 | 0.040 | 10 | 122388123 | intron variant | G/A | snv | 0.47 | 1 | ||
| rs11200629 | 1.000 | 0.040 | 10 | 122439069 | 3 prime UTR variant | A/G | snv | 0.47 | 1 | ||
| rs11200638 | 0.724 | 0.280 | 10 | 122461028 | non coding transcript exon variant | G/A | snv | 0.23 | 1 | ||
| rs17103488 | 1.000 | 0.040 | 10 | 122394653 | intron variant | T/C | snv | 0.11 | 1 | ||
| rs17103522 | 1.000 | 0.040 | 10 | 122418363 | non coding transcript exon variant | T/C | snv | 0.11 | 1 | ||
| rs2014307 | 0.925 | 0.160 | 10 | 122458116 | intron variant | T/G | snv | 0.63 | 1 | ||
| rs2248799 | 1.000 | 0.040 | 10 | 122464428 | intron variant | C/T | snv | 0.51 | 1 |