| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10515789 | 1.000 | 0.040 | 5 | 159079407 | intron variant | T/G | snv | 0.11 | 1 | ||
| rs1278609613 | 1.000 | 0.040 | 4 | 147542604 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 8.0E-06 | 1 | ||
| rs11568953 | 1.000 | 0.040 | 4 | 109963240 | synonymous variant | A/G | snv | 9.7E-03 | 1.0E-02 | 1 | |
| rs781198499 | 1.000 | 0.040 | 5 | 96765321 | missense variant | T/A;C | snv | 7.1E-06 | 1 | ||
| rs202247795 | 1.000 | 0.040 | 2 | 211702102 | missense variant | C/T | snv | 1 | |||
| rs267599192 | 1.000 | 0.040 | 2 | 211673250 | missense variant | G/A | snv | 1 | |||
| rs267599193 | 1.000 | 0.040 | 2 | 211713583 | missense variant | C/T | snv | 1 | |||
| rs535202189 | 1.000 | 0.040 | 2 | 211673256 | missense variant | C/T | snv | 6.8E-05 | 1 | ||
| rs55671017 | 1.000 | 0.040 | 2 | 211705339 | missense variant | G/A;T | snv | 8.0E-06; 6.4E-04 | 1 | ||
| rs776347334 | 1.000 | 0.040 | 2 | 211430974 | missense variant | C/T | snv | 1.2E-05 | 1 | ||
| rs536181987 | 1.000 | 0.040 | 10 | 121503881 | missense variant | G/A | snv | 2.8E-05 | 2.8E-05 | 1 | |
| rs761446954 | 1.000 | 0.040 | 10 | 121496722 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs533045918 | 1.000 | 0.040 | 4 | 1804968 | missense variant | C/G;T | snv | 2.6E-05 | 1 | ||
| rs1269304342 | 1.000 | 0.040 | 10 | 98425560 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs3213119 | 1.000 | 0.040 | 5 | 159316780 | missense variant | C/A | snv | 2.1E-02 | 2.1E-02 | 1 | |
| rs748523570 | 1.000 | 0.040 | 11 | 112150119 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs4845622 | 1.000 | 0.040 | 1 | 154438943 | intron variant | A/C | snv | 0.32 | 1 | ||
| rs868443937 | 1.000 | 0.040 | 13 | 110715751 | missense variant | G/C;T | snv | 1 | |||
| rs759031245 | 1.000 | 0.040 | 9 | 5022025 | missense variant | G/T | snv | 5.2E-05 | 1 | ||
| rs12380505 | 1.000 | 0.040 | 9 | 21695894 | non coding transcript exon variant | A/G | snv | 0.62 | 1 | ||
| rs1057519703 | 1.000 | 0.040 | 4 | 54727418 | missense variant | A/C;T | snv | 1 | |||
| rs1057519705 | 1.000 | 0.040 | 4 | 54727464 | missense variant | A/G | snv | 1 | |||
| rs1057519706 | 1.000 | 0.040 | 4 | 54727474 | missense variant | T/G | snv | 1 | |||
| rs1060502550 | 1.000 | 0.040 | 4 | 54727488 | missense variant | A/G | snv | 1 | |||
| rs121913524 | 1.000 | 0.040 | 4 | 54733182 | missense variant | T/C | snv | 1 |