| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
| rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
| rs1256049 | 0.645 | 0.560 | 14 | 64257333 | synonymous variant | C/T | snv | 6.7E-02 | 6.3E-02 | 32 | |
| rs3025058 | 0.658 | 0.600 | 11 | 102845217 | upstream gene variant | -/C;G | ins | 2.8E-04 | 26 | ||
| rs8179090 | 0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 | 12 | ||
| rs11190870 | 0.827 | 0.200 | 10 | 101219450 | intergenic variant | T/A;C | snv | 6 | |||
| rs6137473 | 0.827 | 0.280 | 20 | 21904055 | intergenic variant | G/A | snv | 0.61 | 5 | ||
| rs1256120 | 0.882 | 0.200 | 14 | 64338283 | non coding transcript exon variant | A/G | snv | 0.20 | 3 | ||
| rs7843033 | 1.000 | 0.040 | 8 | 60759956 | intron variant | A/C;T | snv | 0.77 | 1 | ||
| rs934099 | 1.000 | 0.040 | 19 | 7264916 | intron variant | C/T | snv | 9.7E-02 | 1 | ||
| rs146984380 | 1.000 | 0.040 | 5 | 75685328 | missense variant | G/A | snv | 7.7E-03 | 6.8E-03 | 1 | |
| rs34678567 | 1.000 | 0.040 | 5 | 75685278 | missense variant | C/A;T | snv | 8.0E-06; 1.1E-02 | 1 | ||
| rs763910203 | 1.000 | 0.040 | 5 | 75685251 | missense variant | C/G | snv | 6.4E-05 | 1.0E-04 | 1 | |
| rs2277700 | 1.000 | 0.040 | 17 | 78870629 | intron variant | C/A;G;T | snv | 1 | |||
| rs4789934 | 1.000 | 0.040 | 17 | 78915454 | intron variant | G/A;T | snv | 1 | |||
| rs11658743 | 1.000 | 0.040 | 17 | 78877679 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs2377005 | 1.000 | 0.040 | 17 | 78874211 | intron variant | A/G | snv | 0.93 | 1 |