Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11207997 | 1 | 62596235 | intron variant | C/T | snv | 0.39 | 6 | ||||
rs132630331 | 1.000 | X | 30707584 | missense variant | A/G | snv | 3 | ||||
rs12522383 | 5 | 111119568 | intron variant | G/A | snv | 0.29 | 2 | ||||
rs2074380 | 4 | 112432155 | missense variant | G/A;T | snv | 8.5E-03; 2.4E-05 | 2 | ||||
rs2074381 | 4 | 112432293 | missense variant | A/G | snv | 8.5E-03 | 5.5E-03 | 2 | |||
rs9846911 | 3 | 187500548 | intergenic variant | A/G | snv | 0.47 | 2 | ||||
rs138850469 | 2 | 181678775 | missense variant | G/C | snv | 5.2E-05 | 4.2E-05 | 1 | |||
rs2073932 | 9 | 133440318 | intron variant | A/G | snv | 0.57 | 1 | ||||
rs33929415 | 11 | 5225612 | missense variant | G/A;C;T | snv | 4.0E-06 | 1 | ||||
rs35810727 | 1 | 206112629 | intron variant | G/A;T | snv | 1 | |||||
rs536297956 | 13 | 25530064 | missense variant | C/T | snv | 1 | |||||
rs587783675 | 11 | 17387104 | missense variant | A/G | snv | 1 | |||||
rs652600 | 9 | 133445896 | intron variant | G/A | snv | 0.66 | 1 | ||||
rs7375036 | 3 | 38727881 | intron variant | T/C | snv | 6.4E-03 | 1 | ||||
rs750521766 | 1 | 201389275 | missense variant | C/T | snv | 1.1E-04 | 3.5E-05 | 1 | |||
rs7712562 | 5 | 1295957 | upstream gene variant | A/G | snv | 0.88 | 1 | ||||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 9 | ||
rs62435145 | 1.000 | 0.040 | 7 | 1246931 | regulatory region variant | G/T | snv | 0.51 | 8 | ||
rs3765209 | 0.851 | 0.040 | 21 | 15417030 | intron variant | C/T | snv | 0.31 | 7 | ||
rs4810479 | 1.000 | 0.040 | 20 | 45916409 | upstream gene variant | C/T | snv | 0.68 | 7 | ||
rs13146355 | 1.000 | 0.040 | 4 | 76490987 | intron variant | G/A | snv | 0.33 | 6 | ||
rs11920090 | 1.000 | 0.040 | 3 | 170999732 | intron variant | T/A | snv | 0.20 | 5 | ||
rs12922822 | 1.000 | 0.040 | 16 | 20356323 | upstream gene variant | C/A;T | snv | 5 | |||
rs3789678 | 1.000 | 0.040 | 1 | 230713736 | intron variant | C/T | snv | 0.15 | 5 | ||
rs7936247 | 1.000 | 0.040 | 11 | 92956866 | intergenic variant | G/T | snv | 0.37 | 5 |