Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs635311 0.925 0.040 2 219637645 missense variant A/C;T snv 0.75; 8.0E-06 2
rs2298771 0.925 0.040 2 166036278 missense variant C/T snv 0.73 0.74 3
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs628031 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8
rs2279020 1.000 0.040 5 161895883 non coding transcript exon variant G/A snv 0.62 0.63 2
rs1109771 1.000 0.040 6 32219828 intron variant A/G snv 0.57 0.54 1
rs7439366 0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs25681
C5
0.882 0.120 9 121017727 synonymous variant G/A snv 0.47 0.35 3
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs443198 0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39 4
rs1105879 0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs3740066 0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs2070959 0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs211037 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 14
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135