Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894469 | 0.925 | 0.080 | 14 | 36663043 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
rs104894562 | 0.882 | 0.200 | 17 | 28529157 | stop gained | C/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs1095 | 0.925 | 0.080 | 4 | 4863211 | 3 prime UTR variant | C/T | snv | 1.5E-02 | 2 | ||
rs11001553 | 0.925 | 0.080 | 10 | 52313141 | intron variant | C/T | snv | 0.12 | 2 | ||
rs114632254 | 1.000 | 1 | 236482309 | missense variant | C/T | snv | 2.1E-02 | 2.1E-02 | 1 | ||
rs116998555 | 0.882 | 0.080 | 2 | 218890118 | missense variant | C/A;T | snv | 4.0E-06; 1.9E-03 | 2 | ||
rs11806449 | 1.000 | 1 | 240493497 | intron variant | G/A | snv | 0.21 | 0.17 | 1 | ||
rs121908119 | 0.763 | 0.200 | 2 | 218882368 | stop gained | C/A | snv | 6.2E-04 | 8.5E-04 | 5 | |
rs121908120 | 0.701 | 0.280 | 2 | 218890289 | missense variant | T/A | snv | 1.4E-02 | 1.4E-02 | 4 | |
rs121908568 | 0.807 | 0.160 | 17 | 65536495 | stop gained | G/A | snv | 8 | |||
rs1219648 | 0.716 | 0.320 | 10 | 121586676 | intron variant | A/G;T | snv | 16 | |||
rs12532 | 0.790 | 0.200 | 4 | 4863419 | 3 prime UTR variant | A/G | snv | 0.36 | 10 | ||
rs1292564852 | 1.000 | 4 | 1805414 | missense variant | C/T | snv | 7.0E-06 | 1 | |||
rs1315861554 | 0.925 | 0.120 | 18 | 3457392 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs140920120 | 0.925 | 0.080 | 14 | 53952099 | missense variant | C/A;G | snv | 2.8E-04 | 2 | ||
rs1444216093 | 1.000 | 4 | 5632031 | missense variant | G/A;C | snv | 1 | ||||
rs147680216 | 0.742 | 0.160 | 2 | 218890244 | missense variant | G/A | snv | 2.1E-03 | 6.9E-04 | 9 | |
rs15705 | 1.000 | 20 | 6779333 | 3 prime UTR variant | A/C;T | snv | 1 | ||||
rs17015215 | 1.000 | 1 | 209790735 | missense variant | C/T | snv | 1 | ||||
rs17563 | 0.790 | 0.320 | 14 | 53950804 | stop lost | A/G | snv | 0.45 | 0.44 | 8 | |
rs17576 | 0.557 | 0.760 | 20 | 46011586 | missense variant | A/G | snv | 0.39 | 0.36 | 73 | |
rs1800054 | 0.827 | 0.080 | 11 | 108227849 | missense variant | C/G;T | snv | 7.1E-03 | 7 | ||
rs2235371 | 0.752 | 0.360 | 1 | 209790735 | missense variant | C/T | snv | 8.7E-02 | 3.9E-02 | 11 | |
rs2240308 | 0.701 | 0.360 | 17 | 65558473 | missense variant | G/A | snv | 0.47 | 0.39 | 18 | |
rs2252070 | 0.752 | 0.320 | 11 | 102955810 | upstream gene variant | C/T | snv | 0.68 | 13 |