| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912665 | 1.000 | 0.120 | 17 | 7674965 | missense variant | G/A | snv | 2.4E-05 | 7.0E-06 | 7 | |
| rs121908586 | 1.000 | 0.080 | 4 | 54274869 | missense variant | T/A;C | snv | 5 | |||
| rs1452231640 | 1.000 | 0.080 | 8 | 42339015 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
| rs112295309 | 1.000 | 0.080 | 8 | 143813896 | missense variant | T/C;G | snv | 6.1E-04 | 3 | ||
| rs1259653415 | 1.000 | 0.080 | 3 | 196071416 | missense variant | T/C | snv | 7.0E-06 | 3 | ||
| rs2046463 | 1.000 | 0.080 | 4 | 176681548 | intron variant | G/A;C | snv | 3 | |||
| rs573154688 | 1.000 | 0.160 | 17 | 7670711 | missense variant | C/T | snv | 4.4E-05 | 3.5E-05 | 3 | |
| rs80291436 | 1.000 | 0.080 | X | 7843706 | missense variant | T/A;C;G | snv | 4.9E-05; 0.19 | 3 | ||
| rs113561019 | 1.000 | 0.080 | 3 | 9756791 | missense variant | G/A;T | snv | 3.9E-03; 4.0E-06 | 2 | ||
| rs11777210 | 1.000 | 0.080 | 8 | 1979843 | intron variant | C/G;T | snv | 2 | |||
| rs1356083197 | 1.000 | 0.040 | 1 | 224434068 | missense variant | C/T | snv | 1.5E-05 | 1.4E-05 | 2 | |
| rs1374712964 | 1.000 | 0.080 | 1 | 45332028 | missense variant | T/C | snv | 2 | |||
| rs138106763 | 1.000 | 0.040 | 7 | 100857102 | missense variant | A/G | snv | 7.2E-05 | 1.2E-04 | 2 | |
| rs1390902532 | 1.000 | 0.040 | 9 | 21968766 | missense variant | T/C | snv | 7.4E-06 | 7.0E-06 | 2 | |
| rs1400826115 | 1.000 | 0.080 | 3 | 9756770 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
| rs1670661 | 1.000 | 0.040 | 11 | 21209124 | intron variant | C/G;T | snv | 2 | |||
| rs200817352 | 1.000 | 0.080 | 2 | 113220126 | missense variant | G/A;C | snv | 2.0E-03; 4.0E-06 | 2 | ||
| rs2279398 | 1.000 | 0.080 | 5 | 177503768 | 3 prime UTR variant | C/T | snv | 2.7E-02 | 2 | ||
| rs28936409 | 1.000 | 0.080 | 4 | 110621303 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs373646414 | 1.000 | 0.080 | 14 | 95132574 | missense variant | T/C | snv | 1.6E-05 | 5.6E-05 | 2 | |
| rs397509039 | 1.000 | 0.200 | 17 | 43092379 | missense variant | G/A;C | snv | 2 | |||
| rs57408770 | 1.000 | 0.080 | 2 | 219058688 | non coding transcript exon variant | -/AAG | delins | 2 | |||
| rs587776946 | 1.000 | 1 | 113114471 | stop gained | C/T | snv | 2 | ||||
| rs587781351 | 1.000 | 0.040 | 16 | 68828263 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs72478580 | 1.000 | 5 | 35072610 | missense variant | T/G | snv | 1.9E-02 | 1.9E-02 | 2 |