| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10738760 | 0.807 | 0.320 | 9 | 2691186 | regulatory region variant | A/G | snv | 0.56 | 1 | ||
| rs10830956 | 1.000 | 0.040 | 11 | 92947847 | intergenic variant | C/T | snv | 0.33 | 1 | ||
| rs11600380 | 1.000 | 0.040 | 11 | 116799466 | intergenic variant | T/C | snv | 6.6E-02 | 1 | ||
| rs11986942 | 1.000 | 0.040 | 8 | 20009934 | intergenic variant | C/G;T | snv | 1 | |||
| rs12149545 | 0.851 | 0.080 | 16 | 56959249 | upstream gene variant | G/A | snv | 0.23 | 1 | ||
| rs12545984 | 1.000 | 0.040 | 8 | 19989748 | intergenic variant | C/T | snv | 0.16 | 1 | ||
| rs1423096 | 0.925 | 0.080 | 19 | 7674291 | upstream gene variant | T/C | snv | 0.92 | 1 | ||
| rs1441756 | 1.000 | 0.040 | 8 | 20010875 | intergenic variant | A/C;G;T | snv | 1 | |||
| rs180344 | 1.000 | 0.040 | 11 | 116742468 | regulatory region variant | T/C | snv | 0.34 | 1 | ||
| rs1837842 | 1.000 | 0.040 | 8 | 20010779 | intergenic variant | T/C | snv | 0.23 | 1 | ||
| rs1919484 | 1.000 | 0.040 | 8 | 20012165 | intergenic variant | G/A | snv | 0.23 | 1 | ||
| rs2197089 | 0.925 | 0.080 | 8 | 19968862 | downstream gene variant | G/A | snv | 0.61 | 1 | ||
| rs3093068 | 1.000 | 0.040 | 1 | 159711574 | downstream gene variant | G/C | snv | 0.13 | 1 | ||
| rs4244457 | 1.000 | 0.040 | 8 | 20041535 | intergenic variant | C/G;T | snv | 1 | |||
| rs4442164 | 1.000 | 0.040 | 8 | 20034670 | regulatory region variant | A/G | snv | 0.28 | 1 | ||
| rs4449813 | 1.000 | 0.040 | 8 | 20045809 | intergenic variant | G/A | snv | 0.34 | 1 | ||
| rs4922117 | 1.000 | 0.040 | 8 | 19995075 | regulatory region variant | T/A;C;G | snv | 0.25 | 1 | ||
| rs5945326 | 0.925 | 0.080 | X | 153634467 | regulatory region variant | A/G | snv | 0.25 | 1 | ||
| rs6711016 | 1.000 | 0.040 | 2 | 20923592 | intergenic variant | C/A | snv | 0.19 | 1 | ||
| rs6947830 | 0.925 | 0.080 | 7 | 15025359 | intergenic variant | G/A;C | snv | 1 | |||
| rs7013777 | 1.000 | 0.040 | 8 | 20020845 | intergenic variant | T/C;G | snv | 1 | |||
| rs7461115 | 1.000 | 0.040 | 8 | 20014029 | intergenic variant | C/A;G | snv | 0.37 | 1 | ||
| rs7575840 | 1.000 | 0.040 | 2 | 21050618 | intergenic variant | G/T | snv | 0.26 | 1 | ||
| rs569805 | 1.000 | 0.040 | 2 | 168926370 | intron variant | A/T | snv | 0.73 | 1 | ||
| rs12503643 | 1.000 | 0.040 | 4 | 184824934 | intron variant | G/A;T | snv | 1 |