Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879 0.763 0.280 15 44711548 start lost T/C;G snv 10
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
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
rs149680468 0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519985 0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520005 0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs121913370 0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs148924904 0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs180177040 0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25