| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1250248 | 1.000 | 0.040 | 2 | 215422370 | intron variant | A/G | snv | 0.77 | 4 | ||
| rs7521902 | 1.000 | 0.040 | 1 | 22164231 | intergenic variant | C/A | snv | 0.22 | 4 | ||
| rs1055144 | 1.000 | 0.040 | 7 | 25831489 | non coding transcript exon variant | C/T | snv | 0.16 | 3 | ||
| rs10917151 | 0.925 | 0.040 | 1 | 22096228 | 3 prime UTR variant | G/A | snv | 0.14 | 3 | ||
| rs12037376 | 0.925 | 0.040 | 1 | 22135618 | intron variant | G/A | snv | 0.13 | 3 | ||
| rs1250258 | 1.000 | 0.040 | 2 | 215435462 | intron variant | C/T | snv | 0.79 | 3 | ||
| rs17694933 | 1.000 | 0.040 | 9 | 22164310 | intergenic variant | G/A | snv | 0.50 | 3 | ||
| rs2235529 | 1.000 | 0.040 | 1 | 22123994 | intron variant | C/T | snv | 0.13 | 3 | ||
| rs62355900 | 1.000 | 0.040 | 5 | 56756868 | regulatory region variant | T/C | snv | 0.15 | 3 | ||
| rs7041895 | 1.000 | 0.040 | 9 | 22162795 | intergenic variant | A/C | snv | 0.47 | 3 | ||
| rs71575922 | 0.925 | 0.040 | 6 | 152232879 | intron variant | C/G | snv | 0.12 | 3 | ||
| rs10859871 | 1.000 | 0.040 | 12 | 95318100 | intron variant | A/C | snv | 0.37 | 2 | ||
| rs10902088 | 1.000 | 0.040 | 11 | 1090036 | non coding transcript exon variant | T/C | snv | 0.73 | 2 | ||
| rs11592737 | 0.925 | 0.040 | 10 | 94843657 | intron variant | A/G | snv | 0.21 | 2 | ||
| rs12030576 | 1.000 | 0.040 | 1 | 115274600 | intron variant | G/C;T | snv | 2 | |||
| rs12455952 | 1.000 | 0.040 | 18 | 61173285 | intergenic variant | T/C;G | snv | 0.19 | 2 | ||
| rs222857 | 1.000 | 0.040 | 17 | 7261244 | intron variant | C/A;G;T | snv | 0.52 | 2 | ||
| rs2276248 | 1.000 | 0.040 | 21 | 44259375 | intron variant | T/C | snv | 6.1E-02 | 2 | ||
| rs3020348 | 1.000 | 0.040 | 6 | 151736779 | intron variant | C/A;T | snv | 2 | |||
| rs3920498 | 1.000 | 0.040 | 1 | 22166394 | intergenic variant | G/C | snv | 0.19 | 2 | ||
| rs4141819 | 1.000 | 0.040 | 2 | 67637543 | intron variant | C/T | snv | 0.71 | 2 | ||
| rs7561460 | 1.000 | 0.040 | 2 | 102000742 | intron variant | T/C | snv | 0.43 | 2 | ||
| rs80111889 | 1.000 | 0.040 | 2 | 112809853 | intergenic variant | T/G | snv | 0.26 | 2 | ||
| rs10129516 | 1.000 | 0.040 | 14 | 63133372 | intron variant | T/A;C | snv | 1 | |||
| rs10131751 | 1.000 | 0.040 | 14 | 28212010 | intergenic variant | C/A | snv | 9.2E-02 | 1 |