Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
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
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4580704 0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs11932595 0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs290487 0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs12836771 0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs13412852 0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs4436578 0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs8004664 0.925 0.080 14 89568628 intron variant G/A;C snv 3
rs10515074 0.925 0.120 5 68270365 intron variant A/G;T snv 2
rs3738435 0.925 0.080 1 239907303 intron variant T/C snv 0.23 2
rs8066560 0.925 0.040 17 17824729 intron variant A/G snv 0.64 2
rs9906827 0.925 0.120 17 80691605 intron variant C/A;T snv 2
rs10139403 1.000 0.040 14 100728224 intron variant A/G snv 0.62 1
rs2282018
AVP
1.000 0.040 20 3084303 intron variant C/T snv 0.60 1
rs369841551 0.882 0.120 18 60371884 stop gained G/A;T snv 4.0E-06 3
rs104894006 0.925 0.040 7 44149992 stop gained G/A;T snv 1.2E-05 2
rs1568724014 0.925 0.080 20 44407421 stop gained C/T snv 2
rs193922262
GCK
0.925 0.080 7 44145636 stop gained C/A;G snv 4.3E-06 2
rs556581174
GCK
0.925 0.080 7 44145637 stop gained G/A;C;T snv 2
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246