Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs386699558 0.882 0.080 6 32642624 missense variant GCC/ACA mnv 3
rs9272785 0.882 0.080 6 32642624 missense variant G/A snv 0.18 8.7E-02 3