Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3087456 0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs4774 0.807 0.240 16 10906991 missense variant G/C snv 0.30 0.28 7
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs3761847 0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
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
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36