Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
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
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4580704 0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
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
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57