Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 11
rs121913370 0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs180177040 0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs587777894 0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs121913469 0.763 0.240 17 39723966 missense variant TT/CC mnv 8
rs1057519890 0.807 0.200 17 39723966 missense variant T/A snv 7
rs1057519917 0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs121913470 0.776 0.200 17 39723967 missense variant T/C;G snv 7
rs1057519786 0.882 0.160 X 47566722 missense variant C/G;T snv 3
rs1057519876 0.882 0.160 X 47566721 missense variant T/G snv 3