Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397508638 0.807 0.160 7 117652871 frameshift variant A/-;AA delins 9
rs121908757 0.925 0.160 7 117587799 missense variant A/C snv 4.0E-06 2
rs397508288 0.882 0.200 7 117590409 missense variant A/C;G snv 4.0E-06 2
rs76371115 0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 5
rs397508462 1.000 0.120 7 117606701 missense variant A/C;G;T snv 3.6E-05; 4.0E-06 1
rs75389940 0.882 0.120 7 117627753 missense variant A/G snv 4.0E-06 3
rs1800080 0.925 0.120 7 117534330 missense variant A/G snv 2
rs397508185 0.925 0.120 7 117548684 missense variant A/G snv 2.8E-05 2.8E-05 2
rs758675549 0.925 0.200 7 117530938 missense variant A/G snv 4.0E-06 2
rs191456345 0.925 0.160 7 117536576 missense variant A/G snv 1.8E-04 1.1E-04 1
rs201124247 0.882 0.160 7 117592008 missense variant A/G snv 3.1E-05 1
rs397508731 1.000 0.120 7 117531109 missense variant A/G snv 1
rs397508310 1.000 0.120 7 117591993 missense variant A/G;T snv 1
rs1057516619 1.000 0.120 7 117536669 stop gained A/T snv 1
rs121908758 0.851 0.160 7 117590394 missense variant C/A snv 8.0E-06 7.0E-06 3
rs121909047 0.925 0.160 7 117590355 missense variant C/A snv 1.2E-05 2.1E-05 1
rs76879328 1.000 0.120 7 117540305 missense variant C/A snv 1
rs121908761 0.851 0.160 7 117611717 stop gained C/A;G snv 1.2E-05 1
rs75053309 1.000 0.120 7 117540309 missense variant C/A;G;T snv 1.0E-04 1
rs74551128 0.807 0.160 7 117548795 missense variant C/A;T snv 5.3E-05; 5.7E-05 6
rs121908803 0.925 0.160 7 117535281 missense variant C/A;T snv 4.0E-06 7.0E-06 1
rs121909034 1.000 0.120 7 117603609 stop gained C/A;T snv 1.1E-03 1
rs1800100 0.925 0.160 7 117592169 missense variant C/A;T snv 6.0E-03 6.1E-03 1
rs397508187 0.925 0.160 7 117548746 missense variant C/A;T snv 8.2E-06 1
rs397508211 1.000 0.120 7 117559537 stop gained C/A;T snv 4.0E-06 1