Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs157580 0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs174570 0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs12721046 19 44917997 intron variant G/A snv 0.11 8
rs1864163 0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 7
rs1532624 0.851 0.160 16 56971567 intron variant C/A snv 0.34 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 7