Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs7873784 0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68