Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs3790843 0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 5
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121