Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs174583 0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs2126259 1.000 8 9327636 intron variant T/C snv 0.87 9
rs10758593 0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs10814916 0.851 0.200 9 4293150 intron variant A/C snv 0.57 7
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs11605924 1.000 0.080 11 45851540 intron variant A/C snv 0.39 5
rs11672660 19 45676926 intron variant C/T snv 0.18 0.17 5
rs11920090 1.000 0.040 3 170999732 intron variant T/A snv 0.20 5
rs17168486 1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs2851682 11 61848540 intron variant A/G snv 9.9E-02 5
rs7651090 0.925 0.080 3 185795604 intron variant A/G snv 0.39 5
rs7944584 1.000 0.080 11 47314769 intron variant A/T snv 0.19 5