| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4148087 | 1.000 | 0.040 | 21 | 42202157 | intron variant | G/A;T | snv | 3 | |||
| rs554073050 | 0.925 | 0.040 | 3 | 42263460 | synonymous variant | G/A | snv | 1.2E-05 | 7.0E-06 | 3 | |
| rs1805576 | 1.000 | 0.040 | 3 | 180949777 | intron variant | C/G;T | snv | 0.24 | 3 | ||
| rs17536211 | 1.000 | 0.040 | 4 | 46085716 | intron variant | A/C | snv | 0.14 | 3 | ||
| rs12149074 | 1.000 | 0.040 | 16 | 80071969 | intron variant | C/A;G | snv | 3 | |||
| rs10858583 | 1.000 | 0.040 | 12 | 87334666 | intergenic variant | C/T | snv | 0.79 | 3 | ||
| rs13086738 | 1.000 | 0.040 | 3 | 181080939 | intron variant | A/G | snv | 0.21 | 3 | ||
| rs4854912 | 1.000 | 0.040 | 3 | 181063312 | intron variant | C/T | snv | 0.15 | 3 | ||
| rs12475512 | 2 | 231433365 | downstream gene variant | G/A | snv | 0.47 | 2 | ||||
| rs74566133 | 8 | 133766099 | regulatory region variant | C/T | snv | 2.6E-02 | 2 | ||||
| rs7322916 | 13 | 25433839 | intron variant | G/A;C | snv | 2 | |||||
| rs13077017 | 3 | 58120049 | intron variant | C/T | snv | 0.21 | 2 | ||||
| rs4869317 | 1.000 | 0.040 | 5 | 96956300 | intron variant | T/A | snv | 0.22 | 2 | ||
| rs1356639869 | 1.000 | 0.040 | 7 | 24289527 | missense variant | C/A | snv | 2 | |||
| rs138206701 | 5 | 81110747 | intron variant | A/G | snv | 1.7E-02 | 2 | ||||
| rs61754648 | 2 | 239090026 | missense variant | C/T | snv | 1.4E-03 | 1.8E-03 | 1 | |||
| rs7180942 | 15 | 88131345 | intron variant | T/C | snv | 0.56 | 1 |