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
GK
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
HBB
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
AGT
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