| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs761896295 | 1.000 | 0.080 | 4 | 1804450 | missense variant | G/A | snv | 2.4E-05 | 2.1E-05 | 2 | |
| rs750949764 | 1.000 | 0.040 | 14 | 75280958 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
| rs751478142 | 1.000 | 5 | 138570994 | missense variant | G/A | snv | 2.8E-05 | 1.4E-05 | 2 | ||
| rs11777210 | 1.000 | 0.080 | 8 | 1979843 | intron variant | C/G;T | snv | 2 | |||
| rs587776946 | 1.000 | 1 | 113114471 | stop gained | C/T | snv | 2 | ||||
| rs57408770 | 1.000 | 0.080 | 2 | 219058688 | non coding transcript exon variant | -/AAG | delins | 2 | |||
| rs760583024 | 1.000 | 0.080 | 11 | 18934156 | missense variant | G/A;T | snv | 8.0E-06 | 2 | ||
| rs1374712964 | 1.000 | 0.080 | 1 | 45332028 | missense variant | T/C | snv | 2 | |||
| rs1670661 | 1.000 | 0.040 | 11 | 21209124 | intron variant | C/G;T | snv | 2 | |||
| rs113561019 | 1.000 | 0.080 | 3 | 9756791 | missense variant | G/A;T | snv | 3.9E-03; 4.0E-06 | 2 | ||
| rs1400826115 | 1.000 | 0.080 | 3 | 9756770 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
| rs200817352 | 1.000 | 0.080 | 2 | 113220126 | missense variant | G/A;C | snv | 2.0E-03; 4.0E-06 | 2 | ||
| rs28936409 | 1.000 | 0.080 | 4 | 110621303 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs72478580 | 1.000 | 5 | 35072610 | missense variant | T/G | snv | 1.9E-02 | 1.9E-02 | 2 | ||
| rs771308693 | 8 | 140752306 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 2 | |||
| rs753066745 | X | 81277164 | missense variant | C/T | snv | 1.7E-05 | 9.5E-06 | 2 | |||
| rs138106763 | 1.000 | 0.040 | 7 | 100857102 | missense variant | A/G | snv | 7.2E-05 | 1.2E-04 | 2 | |
| rs863224682 | 1.000 | 0.080 | 17 | 7669655 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
| rs74751600 | 22 | 28695852 | missense variant | T/C | snv | 3 | |||||
| rs4635002 | 0.925 | 0.080 | 10 | 127064415 | intron variant | A/C | snv | 0.92 | 3 | ||
| rs780439043 | 0.925 | 0.080 | 7 | 55205301 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 | 3 | |
| rs1238981206 | 0.925 | 0.080 | 17 | 39724828 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
| rs529365517 | 0.925 | 0.080 | 1 | 212858540 | missense variant | C/T | snv | 3 | |||
| rs538912281 | 0.925 | 0.080 | 9 | 97854657 | missense variant | C/A;G;T | snv | 2.0E-03 | 3 | ||
| rs2046463 | 1.000 | 0.080 | 4 | 176681548 | intron variant | G/A;C | snv | 3 |