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
rs397508146 1.000 0.120 7 117540267 missense variant T/C snv 1
rs397508280 1.000 0.120 7 117590385 missense variant T/C snv 1
rs201978662 1.000 0.120 7 117592004 missense variant G/A snv 7.0E-06 1
rs397508819 1.000 0.120 7 117540170 missense variant G/C;T snv 1
rs34911792 0.925 0.160 7 117627758 missense variant T/G snv 5.0E-03 5.7E-03 1
rs121909020 1.000 0.120 7 117611640 missense variant G/A;C snv 4.0E-06 1
rs397508635 0.925 0.160 7 117480132 missense variant C/A;T snv 1
rs397508316 1.000 0.120 7 117592049 missense variant G/A;C snv 4.1E-06 1
rs121909005 0.851 0.160 7 117587801 missense variant T/A;C;G snv 4.0E-06; 8.0E-06 1
rs200553511 1.000 0.120 7 117610614 missense variant G/A;T snv 4.0E-06 1
rs397508277 1.000 0.120 7 117590379 missense variant A/G snv 1
rs397508272 1.000 0.120 7 117509038 missense variant T/C;G snv 1
rs201124247 0.882 0.160 7 117592008 missense variant A/G snv 3.1E-05 1
rs76371115 0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 1
rs121909040 1.000 0.120 7 117642466 missense variant G/A snv 7.0E-06 1
rs121909037 1.000 0.120 7 117611653 missense variant A/C;G snv 4.0E-06 1
rs150157202 0.925 0.120 7 117592427 missense variant G/A;T snv 1.8E-03 1.7E-03 1
rs121909006 0.925 0.160 7 117590360 missense variant T/A;C;G snv 8.0E-06 1
rs143486492 1.000 0.120 7 117540120 missense variant G/A snv 5.7E-04 5.7E-04 1
rs368505753 0.925 0.160 7 117509069 missense variant C/T snv 3.6E-05 3.5E-05 1
rs397508691 1.000 0.120 7 117665512 missense variant T/A snv 1
rs77409459 0.851 0.160 7 117540243 missense variant C/T snv 2.8E-05 1.4E-05 1
rs77834169 0.851 0.160 7 117530974 missense variant C/A;G;T snv 8.0E-06; 2.0E-05; 2.0E-04 1
rs267606723 0.827 0.200 7 117642451 missense variant G/A;T snv 8.0E-06; 4.0E-06 1