Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs200340021 0.925 0.080 12 14882204 missense variant C/T snv 7.0E-06 3
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs7195830 0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs41507953 0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614