Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs198389 0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs212528 0.925 0.040 1 21259168 intron variant T/C snv 0.12 3
rs213045 0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs3861950 0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs5355 0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14