Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 22 | ||
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 15 | ||
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 14 | ||
rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 13 | ||
rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 11 | |||
rs602633 | 0.851 | 0.080 | 1 | 109278889 | downstream gene variant | T/G | snv | 0.63 | 10 | ||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 8 | |||
rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 8 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 8 | ||
rs17030613 | 1 | 112648185 | intron variant | A/C | snv | 0.19 | 7 | ||||
rs1167998 | 1 | 62465961 | intron variant | C/A | snv | 0.57 | 6 | ||||
rs2642438 | 1 | 220796686 | missense variant | A/G | snv | 0.75 | 0.78 | 6 | |||
rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
rs4970834 | 0.925 | 0.160 | 1 | 109272258 | intron variant | C/T | snv | 0.17 | 0.21 | 6 | |
rs5176 | 1 | 53246137 | 3 prime UTR variant | T/G | snv | 6.4E-04 | 6 | ||||
rs583104 | 1 | 109278685 | downstream gene variant | G/T | snv | 0.63 | 6 | ||||
rs660240 | 1 | 109275216 | 3 prime UTR variant | T/C | snv | 0.75 | 6 | ||||
rs10789117 | 1 | 62606594 | intron variant | A/C;T | snv | 5 | |||||
rs10889353 | 1 | 62652525 | intron variant | A/C;T | snv | 5 | |||||
rs11207997 | 1 | 62596235 | intron variant | C/T | snv | 0.39 | 5 | ||||
rs12042319 | 1.000 | 0.040 | 1 | 62584148 | 3 prime UTR variant | G/A | snv | 0.36 | 5 | ||
rs1321655 | 1 | 160124668 | intron variant | A/G;T | snv | 5 | |||||
rs1748195 | 0.851 | 0.120 | 1 | 62583922 | intron variant | C/G;T | snv | 5 | |||
rs1748197 | 1 | 62590441 | intron variant | G/A | snv | 0.42 | 5 | ||||
rs2131925 | 1 | 62560271 | intron variant | G/T | snv | 0.57 | 5 |