Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1078761 1.000 0.120 20 33288875 missense variant A/C;G snv 4.1E-06; 0.30 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs75527207 0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15
rs1800076 0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 10
rs397508638 0.807 0.160 7 117652871 frameshift variant A/-;AA delins 9
rs75541969 0.827 0.200 7 117614699 missense variant G/C snv 4.0E-04 3.2E-04 9
rs80034486 0.807 0.160 7 117652877 missense variant C/G snv 1.4E-04 1.6E-04 9
rs77932196 0.790 0.280 7 117540270 missense variant G/A;C;T snv 2.4E-05; 2.4E-05 8
rs113857788 0.882 0.160 7 117664780 missense variant G/C;T snv 1.0E-03; 6.0E-05 5
rs121909005 0.851 0.160 7 117587801 missense variant T/A;C;G snv 4.0E-06; 8.0E-06 5
rs74767530 0.851 0.320 7 117627537 stop gained C/T snv 5.6E-05 4.9E-05 5
rs121908757 0.925 0.160 7 117587799 missense variant A/C snv 4.0E-06 3
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs74551128 0.807 0.160 7 117548795 missense variant C/A;T snv 5.3E-05; 5.7E-05 8
rs193922500 0.851 0.160 7 117548798 missense variant T/C snv 2.0E-04 4.9E-05 5
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs2227307 0.851 0.240 4 73740952 intron variant T/G snv 0.45 6
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188