Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519987 0.776 0.280 17 7673810 missense variant A/C snv 10
rs1057519986 0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057519988 0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs876659675 0.807 0.280 17 7674199 missense variant A/C;G;T snv 8
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057520004 0.752 0.240 17 7674884 missense variant A/C;T snv 12