Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs174538 0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21