Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 17
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs75527207 0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 12
rs77010898 0.742 0.280 7 117642566 stop gained G/A;C snv 4.6E-04; 4.0E-06 11
rs1800076 0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 9
rs397508638 0.807 0.160 7 117652871 frameshift variant A/-;AA delins 9
rs75961395 0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 9
rs80034486 0.807 0.160 7 117652877 missense variant C/G snv 1.4E-04 1.6E-04 9
rs113993959 0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 8
rs75541969 0.827 0.200 7 117614699 missense variant G/C snv 4.0E-04 3.2E-04 8
rs77932196 0.790 0.280 7 117540270 missense variant G/A;C;T snv 2.4E-05; 2.4E-05 7
rs74551128 0.807 0.160 7 117548795 missense variant C/A;T snv 5.3E-05; 5.7E-05 6
rs142920240 0.851 0.240 7 117540273 missense variant T/A snv 1.4E-04 7.0E-05 5
rs76371115 0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 5
rs74767530 0.851 0.320 7 117627537 stop gained C/T snv 5.6E-05 4.9E-05 4
rs113857788 0.882 0.160 7 117664780 missense variant G/C;T snv 1.0E-03; 6.0E-05 3
rs11971167 0.882 0.160 7 117642528 missense variant G/A;T snv 1.3E-03 3
rs121908758 0.851 0.160 7 117590394 missense variant C/A snv 8.0E-06 7.0E-06 3
rs121909011 0.807 0.160 7 117540230 missense variant C/T snv 5.6E-05 9.1E-05 3
rs35516286 0.851 0.160 7 117531068 missense variant T/A;C snv 1.8E-03 3
rs74597325 0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 3
rs75389940 0.882 0.120 7 117627753 missense variant A/G snv 4.0E-06 3
rs77409459 0.851 0.160 7 117540243 missense variant C/T snv 2.8E-05 1.4E-05 3
rs80055610 0.851 0.160 7 117587833 missense variant G/A;C snv 2.4E-05 3
rs79282516 0.851 0.160 7 117559509 missense variant G/A;T snv 3