Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908803 0.925 0.160 7 117535281 missense variant C/A;T snv 4.0E-06 7.0E-06 1
rs121908752 0.851 0.160 7 117535285 missense variant T/G snv 1.9E-04 1.3E-04 2
rs397508780 1.000 0.120 7 117535341 missense variant T/C snv 1
rs397508783 0.925 0.160 7 117535363 missense variant T/A snv 2.4E-05 7.0E-06 1
rs191456345 0.925 0.160 7 117536576 missense variant A/G snv 1.8E-04 1.1E-04 1
rs397508804 1.000 0.120 7 117536663 missense variant A/T snv 1.2E-05 1
rs143486492 1.000 0.120 7 117540120 missense variant G/A snv 5.7E-04 5.7E-04 1
rs150691494 1.000 0.120 7 117540132 missense variant A/G snv 2.9E-04 1.8E-04 1
rs397508817 1.000 0.120 7 117540150 missense variant G/A snv 1
rs121909016 1.000 0.120 7 117540163 missense variant C/G snv 1
rs397508819 1.000 0.120 7 117540170 missense variant G/C;T snv 1
rs75763344 0.925 0.160 7 117540171 missense variant G/A;C;T snv 4.0E-06 1
rs121909011 0.807 0.160 7 117540230 missense variant C/T snv 5.6E-05 9.1E-05 2
rs397508139 0.882 0.160 7 117540237 missense variant T/A;C snv 4.0E-06; 4.0E-06 1
rs77409459 0.851 0.160 7 117540243 missense variant C/T snv 2.8E-05 1.4E-05 1
rs397508146 1.000 0.120 7 117540267 missense variant T/C snv 1
rs77932196 0.790 0.280 7 117540270 missense variant G/A;C;T snv 2.4E-05; 2.4E-05 1
rs121908753 0.851 0.160 7 117540285 missense variant G/A snv 2.4E-05 1
rs76879328 1.000 0.120 7 117540305 missense variant C/A snv 1
rs147422190 0.925 0.160 7 117548758 missense variant G/T snv 2.6E-04 3.3E-04 1
rs74551128 0.807 0.160 7 117548795 missense variant C/A;T snv 5.3E-05; 5.7E-05 1
rs397508195 1.000 0.120 7 117548797 missense variant G/C;T snv 1
rs121909009 1.000 0.120 7 117548804 missense variant G/T snv 1
rs79282516 0.851 0.160 7 117559509 missense variant G/A;T snv 1
rs121909017 0.851 0.160 7 117559546 missense variant C/T snv 8.0E-06 1