Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G 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
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs730882026 0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 11
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 11
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10