Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs758420403 | 1.000 | 4 | 5689210 | missense variant | A/C | snv | 4.0E-06 | 1 | |||
rs15705 | 1.000 | 20 | 6779333 | 3 prime UTR variant | A/C;T | snv | 1 | ||||
rs17576 | 0.557 | 0.760 | 20 | 46011586 | missense variant | A/G | snv | 0.39 | 0.36 | 73 | |
rs12532 | 0.790 | 0.200 | 4 | 4863419 | 3 prime UTR variant | A/G | snv | 0.36 | 10 | ||
rs17563 | 0.790 | 0.320 | 14 | 53950804 | stop lost | A/G | snv | 0.45 | 0.44 | 8 | |
rs861019 | 0.925 | 0.120 | 1 | 209802041 | splice region variant | A/G | snv | 0.44 | 2 | ||
rs7802 | 1.000 | 1 | 209785814 | 3 prime UTR variant | A/G | snv | 7.0E-04 | 1 | |||
rs994158401 | 1.000 | 4 | 4860050 | missense variant | A/G | snv | 1.4E-03 | 1.7E-04 | 1 | ||
rs1219648 | 0.716 | 0.320 | 10 | 121586676 | intron variant | A/G;T | snv | 17 | |||
rs121908119 | 0.763 | 0.200 | 2 | 218882368 | stop gained | C/A | snv | 6.2E-04 | 8.5E-04 | 10 | |
rs987525 | 0.807 | 0.160 | 8 | 128933908 | intron variant | C/A | snv | 0.31 | 7 | ||
rs140920120 | 0.925 | 0.080 | 14 | 53952099 | missense variant | C/A;G | snv | 2.8E-04 | 2 | ||
rs116998555 | 0.882 | 0.080 | 2 | 218890118 | missense variant | C/A;T | snv | 4.0E-06; 1.9E-03 | 3 | ||
rs1800054 | 0.827 | 0.080 | 11 | 108227849 | missense variant | C/G;T | snv | 7.1E-03 | 7 | ||
rs243865 | 0.600 | 0.640 | 16 | 55477894 | intron variant | C/T | snv | 0.19 | 48 | ||
rs2252070 | 0.752 | 0.320 | 11 | 102955810 | upstream gene variant | C/T | snv | 0.68 | 13 | ||
rs2235371 | 0.752 | 0.360 | 1 | 209790735 | missense variant | C/T | snv | 8.7E-02 | 3.9E-02 | 11 | |
rs8670 | 0.925 | 0.080 | 4 | 4863149 | 3 prime UTR variant | C/T | snv | 0.22 | 0.23 | 4 | |
rs104894562 | 0.882 | 0.200 | 17 | 28529157 | stop gained | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
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 | ||
rs1315861554 | 0.925 | 0.120 | 18 | 3457392 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs114632254 | 1.000 | 1 | 236482309 | missense variant | C/T | snv | 2.1E-02 | 2.1E-02 | 1 | ||
rs1292564852 | 1.000 | 4 | 1805414 | missense variant | C/T | snv | 7.0E-06 | 1 | |||
rs17015215 | 1.000 | 1 | 209790735 | missense variant | C/T | snv | 1 |