| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs174601 | 0.925 | 0.080 | 11 | 61855668 | non coding transcript exon variant | C/A;T | snv | 12 | |||
| rs9534275 | 0.851 | 0.080 | 13 | 32366208 | intron variant | C/A | snv | 0.52 | 7 | ||
| rs4846914 | 0.925 | 0.080 | 1 | 230159944 | intron variant | G/A | snv | 0.45 | 6 | ||
| rs11513729 | 1.000 | 0.080 | 12 | 111835695 | downstream gene variant | C/T | snv | 0.29 | 5 | ||
| rs2230500 | 0.925 | 0.080 | 14 | 61457521 | missense variant | G/A | snv | 3.1E-02 | 1.6E-02 | 5 | |
| rs35436 | 1.000 | 0.080 | 12 | 115116718 | intergenic variant | C/T | snv | 0.40 | 5 | ||
| rs6698843 | 0.925 | 0.080 | 1 | 109264212 | synonymous variant | C/A;T | snv | 4.0E-06; 0.44 | 5 | ||
| rs7395662 | 0.882 | 0.080 | 11 | 48497341 | downstream gene variant | A/G | snv | 0.56 | 5 | ||
| rs12130333 | 1.000 | 0.080 | 1 | 62726106 | regulatory region variant | C/T | snv | 0.16 | 4 | ||
| rs2287218 | 0.851 | 0.080 | 12 | 109581533 | synonymous variant | C/T | snv | 0.16 | 0.17 | 4 | |
| rs3212335 | 1.000 | 0.080 | 15 | 26766994 | intron variant | C/T | snv | 0.32 | 4 | ||
| rs4845617 | 0.882 | 0.080 | 1 | 154405422 | 5 prime UTR variant | G/A;C | snv | 4 | |||
| rs864265 | 0.925 | 0.080 | 3 | 186836503 | intergenic variant | T/G | snv | 0.86 | 4 | ||
| rs1052053 | 1.000 | 0.080 | 1 | 156232382 | missense variant | A/C;G | snv | 1.0E-03; 0.38 | 3 | ||
| rs11984041 | 0.925 | 0.080 | 7 | 18992312 | intron variant | C/T | snv | 0.13 | 3 | ||
| rs12204590 | 1.000 | 0.080 | 6 | 1337158 | intergenic variant | T/A | snv | 0.14 | 3 | ||
| rs12476527 | 1.000 | 0.080 | 2 | 26692756 | 5 prime UTR variant | G/C;T | snv | 3 | |||
| rs147783135 | 1.000 | 0.080 | 3 | 112081004 | stop gained | C/T | snv | 2.4E-04 | 6.3E-05 | 3 | |
| rs152312 | 0.925 | 0.080 | 5 | 60491989 | non coding transcript exon variant | G/A;T | snv | 3 | |||
| rs1648707 | 0.925 | 0.080 | 3 | 186833922 | intergenic variant | A/C | snv | 0.43 | 3 | ||
| rs191885206 | 1.000 | 0.080 | 19 | 15696024 | missense variant | T/C | snv | 7.0E-04 | 3.1E-04 | 3 | |
| rs1967309 | 0.925 | 0.080 | 16 | 4015582 | non coding transcript exon variant | A/G | snv | 0.51 | 3 | ||
| rs2005108 | 1.000 | 0.080 | 11 | 102899623 | downstream gene variant | C/G;T | snv | 3 | |||
| rs2139733 | 0.925 | 0.080 | 12 | 117288937 | intron variant | T/A | snv | 0.39 | 3 | ||
| rs2208454 | 0.882 | 0.080 | 20 | 14284769 | intron variant | G/C;T | snv | 3 |