Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs1043618 0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 10
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs3825807 0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs4754 0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs1764391 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs3900940 0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs2229116 0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs12347433 0.882 0.040 9 115035318 synonymous variant T/C snv 0.23 0.21 3
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38