Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519915 0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519959 0.882 0.200 11 66063028 missense variant A/C snv 4
rs121913282 0.882 0.040 3 179221072 missense variant A/C snv 1
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 12
rs1057519986 0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs80357243 17 43063885 missense variant A/C;G snv 2
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T 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
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12