Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10766197 0.807 0.240 11 14900334 upstream gene variant G/A;C snv 6
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
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
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs2069718 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3755276 0.925 0.120 2 102361999 intron variant C/T snv 0.45 3
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17