| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs79827531 | 1.000 | 0.040 | 2 | 167752805 | regulatory region variant | G/A | snv | 0.14 | 1 | ||
| rs998884 | 1.000 | 0.040 | 2 | 147782283 | intergenic variant | A/G | snv | 0.37 | 1 | ||
| rs352140 | 0.630 | 0.680 | 3 | 52222681 | synonymous variant | C/A;G;T | snv | 2.0E-05; 0.49 | 42 | ||
| rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
| rs2254298 | 0.701 | 0.200 | 3 | 8760542 | intron variant | G/A | snv | 0.16 | 23 | ||
| rs2710323 | 0.851 | 0.080 | 3 | 52781889 | intron variant | T/C | snv | 0.49 | 0.54 | 7 | |
| rs353547 | 0.925 | 0.080 | 3 | 52234850 | intron variant | T/C | snv | 0.64 | 3 | ||
| rs1248860 | 1.000 | 0.040 | 3 | 84966628 | intron variant | G/A | snv | 0.56 | 2 | ||
| rs4434138 | 1.000 | 0.040 | 3 | 52522874 | missense variant | A/G | snv | 8.0E-06; 0.44 | 0.39 | 2 | |
| rs4684833 | 1.000 | 0.040 | 3 | 11990245 | intergenic variant | C/T | snv | 0.79 | 2 | ||
| rs4687552 | 0.925 | 0.080 | 3 | 52804386 | non coding transcript exon variant | T/C | snv | 0.33 | 2 | ||
| rs76508707 | 1.000 | 0.040 | 3 | 85347899 | intron variant | C/T | snv | 0.43 | 2 | ||
| rs9829032 | 0.925 | 0.080 | 3 | 85634450 | intron variant | A/G | snv | 0.41 | 2 | ||
| rs9854869 | 1.000 | 0.040 | 3 | 85371574 | intron variant | C/A | snv | 0.17 | 2 | ||
| rs13094915 | 1.000 | 0.040 | 3 | 52473703 | intron variant | G/A;C | snv | 1.0E-04; 0.42 | 1 | ||
| rs13324323 | 1.000 | 0.040 | 3 | 166989488 | intergenic variant | C/T | snv | 0.23 | 1 | ||
| rs1368748 | 1.000 | 0.040 | 3 | 85363180 | intron variant | A/G | snv | 0.50 | 1 | ||
| rs1724725 | 1.000 | 0.040 | 3 | 158184607 | intron variant | A/G;T | snv | 1 | |||
| rs2236939 | 1.000 | 0.040 | 3 | 50206077 | intron variant | G/T | snv | 0.10 | 1 | ||
| rs34135146 | 1.000 | 0.040 | 3 | 52279416 | intron variant | G/C | snv | 9.3E-02 | 1 | ||
| rs4405857 | 1.000 | 0.040 | 3 | 65459852 | intron variant | G/A;C | snv | 1 | |||
| rs480330 | 1.000 | 0.040 | 3 | 136310145 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs4856278 | 1.000 | 0.040 | 3 | 85599499 | intron variant | A/G;T | snv | 1 | |||
| rs525773 | 1.000 | 0.040 | 3 | 136217611 | intergenic variant | G/A | snv | 0.51 | 1 | ||
| rs589092 | 1.000 | 0.040 | 3 | 136260856 | intron variant | A/G | snv | 0.43 | 1 |