| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs63750756 | 0.716 | 0.200 | 17 | 46010324 | missense variant | T/G | snv | 2.6E-05 | 23 | ||
| rs63750802 | 0.851 | 0.080 | 14 | 73219144 | missense variant | T/G | snv | 7 | |||
| rs63750050 | 0.925 | 0.080 | 14 | 73198106 | missense variant | T/G | snv | 5 | |||
| rs76763715 | 0.658 | 0.520 | 1 | 155235843 | missense variant | T/C;G | snv | 2.3E-03 | 35 | ||
| rs1289324472 | 0.716 | 0.400 | 1 | 155236354 | missense variant | T/C | snv | 1.4E-05 | 21 | ||
| rs113994099 | 0.827 | 0.240 | 15 | 89320883 | missense variant | T/C | snv | 10 | |||
| rs34015634 | 0.851 | 0.120 | 12 | 40340380 | missense variant | T/C | snv | 3.2E-05 | 1.4E-05 | 8 | |
| rs41549716 | 0.882 | 0.200 | 15 | 89321842 | missense variant | T/C | snv | 6.6E-03 | 7.0E-03 | 4 | |
| rs1290141855 | 1.000 | 0.040 | 16 | 55698539 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs1057518882 | MT | 14598 | missense variant | T/C | snv | 2 | |||||
| rs28940285 | 1.000 | 0.040 | 1 | 20645640 | missense variant | T/C | snv | 1.6E-05 | 3.5E-05 | 2 | |
| rs63750680 | 1.000 | 0.080 | 14 | 73198076 | missense variant | T/C | snv | 2 | |||
| rs748705829 | 11 | 233109 | missense variant | T/C | snv | 8.0E-06 | 1 | ||||
| rs63751032 | 0.851 | 0.080 | 14 | 73219156 | missense variant | T/A;G | snv | 7 | |||
| rs143624519 | 0.724 | 0.240 | 17 | 45991484 | missense variant | G/A;T | snv | 1.5E-03; 1.2E-05 | 17 | ||
| rs774005786 | 0.790 | 0.080 | 1 | 7970951 | missense variant | G/A;T | snv | 3.9E-04; 2.0E-05 | 8 | ||
| rs112176450 | 0.807 | 0.080 | 3 | 184327401 | missense variant | G/A;T | snv | 2.1E-04 | 2.8E-04 | 7 | |
| rs1426868527 | 1 | 20633841 | missense variant | G/A;T | snv | 3 | |||||
| rs63751165 | 0.925 | 0.120 | 17 | 46010401 | missense variant | G/A;T | snv | 3 | |||
| rs774457232 | 0.925 | 0.080 | 3 | 184331303 | missense variant | G/A;T | snv | 6.4E-05 | 3 | ||
| rs752804472 | 20 | 31484309 | missense variant | G/A;T | snv | 5.7E-06; 5.7E-06 | 1 | ||||
| rs781652026 | 10 | 100989789 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||||
| rs2942168 | 0.925 | 0.120 | 17 | 45637484 | non coding transcript exon variant | G/A;C;T | snv | 0.14 | 4 | ||
| rs5569 | 0.742 | 0.280 | 16 | 55697923 | synonymous variant | G/A;C | snv | 0.31; 4.0E-06 | 19 | ||
| rs367543041 | 0.742 | 0.200 | 1 | 11022553 | missense variant | G/A;C | snv | 3.0E-05 | 15 |