Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519910 0.851 0.160 19 4117551 missense variant A/C;T snv 4
rs1057519882 0.807 0.200 9 21974678 missense variant C/A snv 7
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057519881 0.776 0.240 9 21971111 missense variant T/C snv 8
rs1057520004 0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 22
rs121913385 0.763 0.240 9 21971112 missense variant G/A;C snv 9
rs34968276 0.776 0.240 9 21971110 stop gained G/A;C;T snv 9
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 15
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs121434498 0.807 0.280 19 4117553 missense variant A/C;G;T snv 6
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
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs80338963 0.776 0.280 18 51065548 missense variant C/A;G;T snv 11
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 33
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26