Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs12413409 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs2470890 0.742 0.320 15 74755085 synonymous variant T/C snv 0.57 12
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111