Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1056534 0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 5
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3918188 0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5030718 0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs758130759 0.925 0.120 17 37699149 missense variant C/T snv 1.6E-05 1.4E-05 3
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262