Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs505151 | 0.732 | 0.360 | 1 | 55063514 | missense variant | G/A | snv | 0.95 | 0.90 | 2 | |
rs6689306 | 0.925 | 0.080 | 1 | 154423470 | intron variant | A/G | snv | 0.61 | 2 | ||
rs9970807 | 0.925 | 0.080 | 1 | 56499992 | intron variant | C/T | snv | 0.11 | 2 | ||
rs10909862 | 1.000 | 0.040 | 1 | 3020251 | upstream gene variant | G/A;C;T | snv | 1 | |||
rs11204666 | 1.000 | 0.040 | 1 | 150570652 | intron variant | C/G;T | snv | 1 | |||
rs11204892 | 1.000 | 0.040 | 1 | 151795572 | upstream gene variant | A/G;T | snv | 1 | |||
rs116161686 | 1.000 | 0.040 | 1 | 210300277 | upstream gene variant | G/A | snv | 9.3E-02 | 1 | ||
rs11806316 | 1.000 | 0.040 | 1 | 115210861 | regulatory region variant | G/A | snv | 0.26 | 1 | ||
rs11809443 | 1.000 | 0.040 | 1 | 228138791 | upstream gene variant | T/C | snv | 0.22 | 1 | ||
rs11810571 | 1.000 | 0.040 | 1 | 151789832 | intron variant | C/A;G | snv | 1 | |||
rs12753816 | 1.000 | 0.040 | 1 | 169183350 | intron variant | C/T | snv | 0.24 | 1 | ||
rs147055617 | 1.000 | 0.040 | 1 | 56520631 | intron variant | A/G | snv | 8.3E-02 | 1 | ||
rs1692580 | 1.000 | 0.040 | 1 | 2226509 | upstream gene variant | T/A;C | snv | 1 | |||
rs17416285 | 1.000 | 0.040 | 1 | 56554977 | intron variant | C/A;G;T | snv | 1 | |||
rs17465982 | 1.000 | 0.040 | 1 | 222664597 | intron variant | G/A | snv | 0.57 | 1 | ||
rs1892094 | 1.000 | 0.040 | 1 | 169125221 | intron variant | C/T | snv | 0.41 | 1 | ||
rs198389 | 0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 | 1 | ||
rs2133189 | 0.925 | 0.040 | 1 | 222641100 | intron variant | C/T | snv | 0.56 | 1 | ||
rs2281719 | 1.000 | 0.040 | 1 | 230161913 | intron variant | C/T | snv | 0.45 | 1 | ||
rs2493298 | 1.000 | 0.040 | 1 | 3409348 | intron variant | C/A | snv | 0.14 | 1 | ||
rs2516839 | 0.732 | 0.320 | 1 | 161043331 | 5 prime UTR variant | C/T | snv | 0.49 | 1 | ||
rs2843152 | 1.000 | 0.040 | 1 | 2314131 | upstream gene variant | C/G | snv | 0.65 | 1 | ||
rs3091244 | 0.724 | 0.280 | 1 | 159714875 | upstream gene variant | G/A;T | snv | 1 | |||
rs34091558 | 1.000 | 0.040 | 1 | 201917642 | intron variant | A/- | delins | 0.25 | 1 | ||
rs35158675 | 1.000 | 0.040 | 1 | 222656208 | intron variant | G/A;C | snv | 1 |