Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs371074389 0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs766914563 0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799930 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 17
rs1799931 0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02 14
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121434595 0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2735383 0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs1982151 0.807 0.120 9 84002350 missense variant A/G;T snv 0.73 9
rs55829688 0.827 0.200 1 173868168 5 prime UTR variant T/C;G snv 5
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30