Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267608023 1.000 0.160 2 47482936 missense variant A/C snv 1
rs63750571 1.000 0.160 2 47480770 missense variant A/C;G snv 4.0E-06; 4.0E-06 1
rs63750797 1.000 0.160 2 47480795 missense variant A/C;G snv 1.2E-05; 4.0E-06 1
rs63750838 1.000 0.160 2 47466801 missense variant A/C;G snv 1
rs63751107 1.000 0.160 2 47403288 missense variant A/C;G snv 6.7E-05; 1.3E-05 1
rs17217772 0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 1
rs201118107 1.000 0.160 2 47471051 missense variant A/C;G;T snv 8.0E-06; 1.0E-04; 1.2E-05 1
rs63749936 1.000 0.160 2 47412414 missense variant A/C;G;T snv 4.0E-06; 8.0E-06 1
rs63750881 0.925 0.160 2 47412504 stop gained A/C;G;T snv 1
rs63751656 0.925 0.160 2 47466807 stop gained A/C;G;T snv 1
rs63750716 0.925 0.160 2 47410232 missense variant A/G snv 4.7E-04 1.3E-04 2
rs1085308057 0.925 0.160 2 47475244 missense variant A/G snv 1
rs1553350676 1.000 0.160 2 47410143 missense variant A/G snv 1
rs267607938 1.000 0.160 2 47416344 missense variant A/G snv 8.0E-06 2.8E-05 1
rs267607981 1.000 0.160 2 47475177 missense variant A/G snv 1
rs41295288 1.000 0.160 2 47475052 missense variant A/G snv 3.2E-04 2.2E-04 1
rs55778204 0.925 0.160 2 47470993 missense variant A/G snv 2.3E-04 7.7E-05 1
rs587779116 1.000 0.160 2 47475181 missense variant A/G snv 1
rs61756468 1.000 0.160 2 47475151 missense variant A/G snv 1.2E-03 4.1E-04 1
rs63749841 1.000 0.160 2 47478498 missense variant A/G snv 1.2E-05 7.0E-06 1
rs63750027 1.000 0.160 2 47480753 missense variant A/G snv 2.4E-05 4.2E-05 1
rs63750327 1.000 0.160 2 47410320 missense variant A/G snv 1
rs63750350 1.000 0.160 2 47482801 missense variant A/G snv 1
rs63750887 1.000 0.160 2 47408482 missense variant A/G;T snv 4.0E-06 7.0E-06 1
rs63751232 1.000 0.160 2 47476372 missense variant A/G;T snv 1