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
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs140693 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 10
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2075786 0.790 0.360 5 1266195 intron variant A/G snv 0.55 8
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs969129 0.851 0.200 5 35861166 intron variant T/A;G snv 4
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47