| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35874116 | 1.000 | 0.040 | 1 | 18854899 | missense variant | T/C | snv | 0.29 | 0.31 | 3 | |
| rs3737665 | 0.925 | 0.080 | 1 | 8970905 | missense variant | C/G;T | snv | 4.0E-06; 0.26 | 3 | ||
| rs10864376 | 0.925 | 0.080 | 1 | 8970313 | intron variant | C/A;T | snv | 2 | |||
| rs12138897 | 0.925 | 0.080 | 1 | 8971844 | intron variant | C/A;G;T | snv | 2 | |||
| rs17032907 | 0.925 | 0.040 | 1 | 8950346 | intron variant | C/T | snv | 0.17 | 2 | ||
| rs2274328 | 0.925 | 0.040 | 1 | 8949385 | missense variant | A/C | snv | 0.49 | 0.51 | 2 | |
| rs307355 | 0.925 | 0.080 | 1 | 1329774 | upstream gene variant | T/C | snv | 0.81 | 2 | ||
| rs11166135 | 1.000 | 0.040 | 1 | 98883280 | intergenic variant | A/G | snv | 0.10 | 1 | ||
| rs2046850 | 1.000 | 0.040 | 1 | 210130974 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs2337359 | 1.000 | 0.040 | 1 | 151523320 | intron variant | T/C | snv | 0.30 | 1 | ||
| rs3820640 | 1.000 | 0.040 | 1 | 226681217 | intron variant | T/C | snv | 0.12 | 1 | ||
| rs3896439 | 1.000 | 0.040 | 1 | 4608610 | intergenic variant | G/A | snv | 9.4E-02 | 1 | ||
| rs4971099 | 1.000 | 0.040 | 1 | 155183132 | intron variant | A/C;G;T | snv | 1 | |||
| rs6680186 | 1.000 | 0.040 | 1 | 8979645 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
| rs72694438 | 1.000 | 0.040 | 1 | 103822256 | intergenic variant | G/A | snv | 0.18 | 1 | ||
| rs9308447 | 1.000 | 0.040 | 1 | 9372331 | downstream gene variant | C/T | snv | 0.27 | 1 | ||
| rs9701796 | 1.000 | 0.040 | 1 | 18859635 | missense variant | G/C | snv | 0.78 | 0.79 | 1 | |
| rs9793739 | 1.000 | 0.040 | 1 | 229150111 | intron variant | G/A | snv | 9.6E-02 | 1 | ||
| rs1143627 | 0.605 | 0.760 | 2 | 112836810 | 5 prime UTR variant | G/A | snv | 0.56 | 47 | ||
| rs121908120 | 0.701 | 0.280 | 2 | 218890289 | missense variant | T/A | snv | 1.4E-02 | 1.4E-02 | 19 | |
| rs11676272 | 1.000 | 0.040 | 2 | 24918669 | missense variant | A/G | snv | 0.47 | 0.57 | 5 | |
| rs62106258 | 1.000 | 0.040 | 2 | 417167 | upstream gene variant | T/C | snv | 2.9E-02 | 5 | ||
| rs10180496 | 1.000 | 0.040 | 2 | 12828774 | intron variant | A/G | snv | 0.15 | 1 | ||
| rs1594318 | 1.000 | 0.040 | 2 | 3686354 | intron variant | C/G;T | snv | 1 | |||
| rs263771 | 1.000 | 0.040 | 2 | 185056965 | intergenic variant | C/A;T | snv | 1 |