Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1555206402 0.790 0.320 11 119093274 stop lost GCCCATTAACTGGTTTGTGGGGCACAGATGCCTGGGTTGCTGCTGTCCAGTGCCT/- delins 26
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs12218 0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11
rs6903956 0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs121907892 0.807 0.240 11 64593747 stop gained G/A;C snv 2.8E-04 8
rs33972313 0.790 0.160 5 139379813 missense variant C/A;G;T snv 4.0E-06; 2.7E-02 8
rs16890979 0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 7
rs6855911 0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs143709408 0.882 0.200 11 2527999 missense variant C/T snv 1.6E-04 3.6E-04 5
rs186459505 0.925 0.120 3 52907083 missense variant G/A;T snv 1.1E-04; 4.0E-06 5
rs11231825 0.827 0.240 11 64592802 synonymous variant T/C snv 0.57 0.51 5
rs149454410 0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5