Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs3808607 0.716 0.400 8 58500365 upstream gene variant G/T snv 0.55 16
rs3798577 0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16