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
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 22
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
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
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
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
rs121913485 0.716 0.400 4 1804372 missense variant A/G snv 8
rs1057519890 0.807 0.200 17 39723966 missense variant T/A snv 7
rs121913470 0.776 0.200 17 39723967 missense variant T/C;G snv 7