| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10896450 | 1.000 | 0.080 | 11 | 69240647 | regulatory region variant | A/G | snv | 0.55 | 1 | ||
| rs11006207 | 1.000 | 0.080 | 10 | 46057646 | regulatory region variant | A/G | snv | 0.45 | 1 | ||
| rs11135762 | 1.000 | 0.080 | 8 | 23633678 | downstream gene variant | G/A | snv | 0.65 | 1 | ||
| rs114918764 | 1.000 | 0.080 | 4 | 116449550 | intergenic variant | C/T | snv | 2.0E-03 | 1 | ||
| rs11577139 | 1.000 | 0.080 | 1 | 98200569 | intergenic variant | C/A;T | snv | 1 | |||
| rs11988857 | 1.000 | 0.080 | 8 | 127519628 | intergenic variant | G/A | snv | 0.80 | 1 | ||
| rs12537079 | 1.000 | 0.080 | 7 | 118064652 | intergenic variant | T/A;G | snv | 1 | |||
| rs12799883 | 1.000 | 0.080 | 11 | 69243184 | intergenic variant | T/G | snv | 0.51 | 1 | ||
| rs1398240 | 1.000 | 0.080 | 8 | 23644093 | intergenic variant | C/A | snv | 0.55 | 1 | ||
| rs1419040 | 1.000 | 0.080 | X | 51609183 | intergenic variant | G/A | snv | 1 | |||
| rs2611512 | 1.000 | 0.080 | 10 | 46080288 | regulatory region variant | T/C | snv | 0.49 | 1 | ||
| rs365586 | 1.000 | 0.080 | 14 | 39984510 | intron variant | G/A;C | snv | 0.38 | 1 | ||
| rs395080 | 1.000 | 0.080 | 14 | 39982929 | intron variant | C/A;T | snv | 1 | |||
| rs417245 | 1.000 | 0.080 | 14 | 39978496 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs4604628 | 1.000 | 0.080 | X | 51644318 | intergenic variant | C/G;T | snv | 1 | |||
| rs4999155 | 1.000 | 0.080 | 9 | 81848028 | regulatory region variant | C/T | snv | 0.11 | 1 | ||
| rs66504230 | 1.000 | 0.080 | 6 | 86161726 | intergenic variant | T/C | snv | 0.11 | 1 | ||
| rs7017300 | 1.000 | 0.080 | 8 | 127513023 | regulatory region variant | C/A | snv | 0.81 | 1 | ||
| rs705308 | 1.000 | 0.080 | 7 | 98066051 | intergenic variant | C/A;T | snv | 1 | |||
| rs7918885 | 1.000 | 0.080 | 10 | 8432632 | intron variant | T/G | snv | 0.26 | 1 | ||
| rs9656816 | 1.000 | 0.080 | 8 | 127522409 | intergenic variant | G/A | snv | 0.94 | 1 | ||
| rs985081 | 1.000 | 0.080 | X | 149456568 | intergenic variant | T/C | snv | 0.14 | 1 | ||
| rs10931777 | 1.000 | 0.080 | 2 | 197278867 | intron variant | C/T | snv | 0.72 | 1 | ||
| rs6727480 | 1.000 | 0.080 | 2 | 197279147 | intron variant | A/G | snv | 0.19 | 1 | ||
| rs138454018 | 1.000 | 0.080 | X | 67546171 | missense variant | C/A;T | snv | 4.4E-05; 4.9E-05 | 1 |