Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 171
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs759834365 0.471 0.679 11 27658456 missense variant C/T snp 1.2E-05 157
rs4680 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 155
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 74
rs662 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 71
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs1801394 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 60
rs1799971 0.611 0.500 6 154039662 missense variant A/G snp 0.19 0.12 57
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 50
rs2234693 0.590 0.571 6 151842200 intron variant T/C snp 0.47 50
rs6313 0.590 0.500 13 46895805 synonymous variant G/A snp 0.41 0.39 50
rs34637584 0.630 0.321 12 40340400 missense variant G/A snp 5.3E-04 1.9E-04 47
rs4994 0.605 0.536 8 37966280 missense variant A/G snp 0.11 9.0E-02 44
rs25531 0.626 0.321 17 30237328 intergenic variant T/C snp 39
rs9340799 0.611 0.607 6 151842246 intron variant A/G snp 0.31 37
rs1800497 0.662 0.250 11 113400106 missense variant G/A snp 0.26 0.26 36
rs6295 0.667 0.179 5 63962738 intron variant C/G snp 0.49 32
rs1006737 0.679 0.107 12 2236129 intron variant G/A snp 0.37 31
rs1205
CRP
0.652 0.500 1 159712443 3 prime UTR variant C/T snp 0.32 30
rs1501299 0.647 0.536 3 186853334 intron variant G/C,T snp 6.4E-05; 0.30 28
rs16139 0.657 0.500 7 24285260 missense variant T/A,C snp 4.0E-06; 3.0E-02 3.2E-02 27
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 27
rs1049353 0.657 0.464 6 88143916 synonymous variant C/T snp 0.21 0.20 26