Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 1
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 1
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7