Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs10774625 0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs5744292 0.851 0.200 11 112143413 3 prime UTR variant T/C snv 0.16 4
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs5063 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2781666 0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs7830 0.763 0.320 7 151012483 3 prime UTR variant G/T snv 0.38 0.32 11
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57