Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23