| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10055201 | 0.882 | 0.080 | 5 | 55865274 | intron variant | A/G | snv | 0.76 | 3 | ||
| rs10131293 | 1.000 | 0.040 | 14 | 22461166 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs10132733 | 1.000 | 0.040 | 14 | 22477241 | intron variant | A/G | snv | 0.19 | 1 | ||
| rs10142552 | 1.000 | 0.040 | 14 | 22395232 | intron variant | G/A | snv | 3.5E-02 | 1 | ||
| rs10148895 | 1.000 | 0.040 | 14 | 22254840 | intron variant | C/T | snv | 0.18 | 1 | ||
| rs10155916 | 1.000 | 0.040 | 7 | 38286177 | intergenic variant | G/A | snv | 0.11 | 1 | ||
| rs10162417 | 1.000 | 0.040 | 14 | 22460708 | intron variant | T/G | snv | 0.15 | 1 | ||
| rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
| rs1027702 | 0.882 | 0.080 | 1 | 161743067 | intergenic variant | C/T | snv | 0.51 | 3 | ||
| rs1039659576 | 0.689 | 0.520 | 1 | 236803473 | missense variant | A/G | snv | 21 | |||
| rs1040303 | 1.000 | 0.040 | 14 | 22403377 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
| rs10441090 | 1.000 | 0.040 | 7 | 38295217 | upstream gene variant | C/T | snv | 0.13 | 1 | ||
| rs1045485 | 0.637 | 0.480 | 2 | 201284866 | missense variant | G/A;C;T | snv | 4.0E-06; 9.0E-02 | 34 | ||
| rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
| rs1048108 | 0.827 | 0.120 | 2 | 214809500 | missense variant | G/A | snv | 0.38 | 0.33 | 5 | |
| rs10483273 | 1.000 | 0.040 | 14 | 22448054 | intron variant | A/G | snv | 9.5E-02 | 1 | ||
| rs10483275 | 1.000 | 0.040 | 14 | 22464064 | intron variant | C/T | snv | 9.5E-02 | 1 | ||
| rs10483277 | 1.000 | 0.040 | 14 | 22471852 | intron variant | C/G;T | snv | 1 | |||
| rs10487742 | 1.000 | 0.040 | 7 | 38326911 | non coding transcript exon variant | G/A | snv | 0.14 | 1 | ||
| rs104893855 | 0.851 | 0.160 | 4 | 41747479 | missense variant | C/A | snv | 4 | |||
| rs104893856 | 0.827 | 0.080 | 4 | 41746162 | missense variant | C/T | snv | 6 | |||
| rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
| rs104893878 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 21 | |||
| rs104893936 | 0.851 | 0.120 | 5 | 176626472 | missense variant | C/G;T | snv | 5.6E-05 | 4 |