Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40