Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 14
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 10
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 16
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 33
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 19
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs398124146 0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 12