| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs117565607 | 1.000 | 0.120 | 6 | 30204594 | intron variant | T/A | snv | 2.3E-03 | 1 | ||
| rs11865086 | 1.000 | 0.120 | 16 | 30119172 | intron variant | C/A | snv | 0.55 | 1 | ||
| rs13299349 | 1.000 | 0.120 | 9 | 18573362 | mature miRNA variant | G/A | snv | 0.32 | 0.27 | 1 | |
| rs1373589952 | 1.000 | 0.120 | 1 | 206772296 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs1407019 | 1.000 | 0.120 | 20 | 33237991 | intron variant | G/A | snv | 0.27 | 1 | ||
| rs1536826 | 1.000 | 0.120 | 10 | 133543735 | intron variant | A/C | snv | 0.62 | 1 | ||
| rs1610588 | 1.000 | 0.120 | 6 | 29708939 | upstream gene variant | C/T | snv | 0.19 | 1 | ||
| rs1610742 | 1.000 | 0.120 | 6 | 29710175 | upstream gene variant | T/C | snv | 0.19 | 1 | ||
| rs16896923 | 1.000 | 0.120 | 6 | 30032910 | non coding transcript exon variant | T/C | snv | 5.0E-02 | 1 | ||
| rs169111 | 1.000 | 0.120 | 3 | 37474042 | intron variant | C/T | snv | 0.84 | 1 | ||
| rs169188 | 1.000 | 0.120 | 3 | 37465958 | intron variant | G/A | snv | 7.6E-02 | 1 | ||
| rs17046583 | 1.000 | 0.120 | 2 | 55001811 | intron variant | A/G | snv | 6.8E-02 | 1 | ||
| rs197757 | 1.000 | 0.120 | 3 | 37481337 | intron variant | G/A | snv | 0.14 | 1 | ||
| rs2074517 | 1.000 | 0.120 | 17 | 34997659 | non coding transcript exon variant | T/C | snv | 2.1E-02 | 1 | ||
| rs2212020 | 1.000 | 0.120 | 3 | 37475971 | intron variant | C/T | snv | 0.34 | 1 | ||
| rs2275531 | 1.000 | 0.120 | 1 | 206935771 | missense variant | C/G;T | snv | 0.38 | 1 | ||
| rs2279244 | 1.000 | 0.120 | 12 | 75502884 | 3 prime UTR variant | C/T | snv | 0.23 | 1 | ||
| rs232228 | 1.000 | 0.120 | 2 | 88859459 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs232230 | 1.000 | 0.120 | 2 | 88857435 | missense variant | C/G | snv | 0.14 | 0.17 | 1 | |
| rs2588519 | 1.000 | 0.120 | 2 | 54977988 | intron variant | T/C | snv | 0.68 | 1 | ||
| rs2735845 | 1.000 | 0.120 | 5 | 1300469 | intergenic variant | C/G | snv | 0.16 | 1 | ||
| rs2752903 | 1.000 | 0.120 | 20 | 33235584 | upstream gene variant | T/C;G | snv | 0.33 | 1 | ||
| rs291102 | 1.000 | 0.120 | 1 | 206933133 | missense variant | G/A;C | snv | 0.10 | 1 | ||
| rs2920891 | 1.000 | 0.120 | 2 | 55080901 | intron variant | C/A;T | snv | 1 | |||
| rs29218 | 1.000 | 0.120 | 6 | 29639652 | upstream gene variant | A/G | snv | 0.17 | 1 |