Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs5744168 0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs352139 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs28940579 0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 13
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs7708392 0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs8193037 0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs6478109 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12