Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519959 0.882 0.200 11 66063028 missense variant A/C snv 4
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
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 13
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057519997 0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 30
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs1057520005 0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 37
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15