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
rs688 0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2259816 0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 8
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
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
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48