| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10080 | 1.000 | 0.080 | 10 | 33178180 | 3 prime UTR variant | G/A | snv | 0.50 | 1 | ||
| rs104893902 | 0.925 | 0.080 | 5 | 173232888 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
| rs104893904 | 0.807 | 0.160 | 5 | 173235023 | missense variant | C/G | snv | 1.1E-03 | 7.1E-04 | 6 | |
| rs104893905 | 0.925 | 0.080 | 5 | 173232898 | missense variant | G/A | snv | 4.4E-06 | 2 | ||
| rs1057515420 | 1.000 | 0.080 | 7 | 100819874 | missense variant | G/A | snv | 1 | |||
| rs11065987 | 0.807 | 0.280 | 12 | 111634620 | intergenic variant | A/G | snv | 0.29 | 17 | ||
| rs11066188 | 0.851 | 0.320 | 12 | 112172910 | intron variant | G/A;C | snv | 0.30; 4.1E-06 | 7 | ||
| rs11066320 | 0.925 | 0.120 | 12 | 112468611 | intron variant | A/G | snv | 0.70 | 5 | ||
| rs1114167357 | 1.000 | 0.080 | 15 | 63042945 | splice donor variant | T/C | snv | 1 | |||
| rs1131695 | 1.000 | 0.080 | 20 | 10652589 | stop gained | G/A;C;T | snv | 0.46 | 1 | ||
| rs115099192 | 0.827 | 0.080 | 8 | 11758366 | missense variant | C/A;G | snv | 5.1E-04; 6.8E-05 | 5 | ||
| rs115875978 | 1.000 | 0.080 | 15 | 58010691 | missense variant | C/A;T | snv | 5.9E-04; 4.0E-06 | 1 | ||
| rs1185861796 | 1.000 | 0.080 | 8 | 11758339 | missense variant | C/A | snv | 8.0E-06 | 7.0E-06 | 2 | |
| rs121434424 | 1.000 | 0.080 | 19 | 18869231 | missense variant | C/A;T | snv | 2.1E-04 | 1 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs121908601 | 0.851 | 0.080 | 8 | 105419192 | missense variant | A/C;G | snv | 4.0E-06; 2.7E-03 | 4 | ||
| rs121908603 | 0.882 | 0.120 | 8 | 105802189 | missense variant | A/C;G | snv | 4.9E-04; 4.0E-06 | 3 | ||
| rs121918351 | 0.882 | 0.240 | 20 | 10658611 | missense variant | C/T | snv | 3 | |||
| rs1222213359 | 0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv | 62 | |||
| rs12519770 | 1.000 | 0.080 | 5 | 90777460 | intron variant | A/G | snv | 0.40 | 1 | ||
| rs139365823 | 0.925 | 0.080 | 16 | 56858519 | non coding transcript exon variant | G/A;C;T | snv | 4.1E-06; 2.9E-05 | 2 | ||
| rs1445910672 | 1.000 | 0.080 | 22 | 19761255 | stop gained | G/A;T | snv | 1 | |||
| rs1448468136 | 1.000 | 0.080 | 8 | 105802610 | missense variant | C/A;T | snv | 1 | |||
| rs145895196 | 0.925 | 0.120 | 20 | 10641566 | missense variant | C/A;T | snv | 1.6E-05; 1.9E-03 | 2 | ||
| rs149655951 | 1.000 | 0.080 | 15 | 57992742 | missense variant | A/G | snv | 4.0E-06 | 1 |