Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38