Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17217772 0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 1
rs17224367 0.882 0.160 2 47429833 missense variant C/G;T snv 1.5E-03 2
rs61756468 1.000 0.160 2 47475151 missense variant A/G snv 1.2E-03 4.1E-04 1
rs63750716 0.925 0.160 2 47410232 missense variant A/G snv 4.7E-04 1.3E-04 2
rs63750124 1.000 0.160 2 47410162 missense variant T/G snv 3.2E-04 3.1E-04 1
rs41295288 1.000 0.160 2 47475052 missense variant A/G snv 3.2E-04 2.2E-04 1
rs34136999 1.000 0.160 2 47414291 missense variant C/T snv 3.0E-04 4.5E-04 1
rs55778204 0.925 0.160 2 47470993 missense variant A/G snv 2.3E-04 7.7E-05 1
rs33946261 1.000 0.160 2 47403329 missense variant C/G;T snv 2.2E-04 1.8E-04 1
rs63750466 1.000 0.160 2 47403195 missense variant G/A snv 1.5E-04 7.7E-05 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
rs63750757 1.000 0.160 2 47480737 missense variant G/A snv 9.9E-05 7.7E-05 1
rs63750617 0.851 0.160 2 47803473 missense variant C/G;T snv 4.0E-06; 9.5E-05 1
rs63750255 1.000 0.160 2 47410226 missense variant G/C snv 8.7E-05 7.0E-05 1
rs267608022 0.925 0.200 2 47482858 missense variant C/G;T snv 8.0E-06; 8.4E-05 1
rs63751107 1.000 0.160 2 47403288 missense variant A/C;G snv 6.7E-05; 1.3E-05 1
rs63751454 1.000 0.160 2 47414389 missense variant G/A snv 6.0E-05 7.9E-05 1
rs63750790 1.000 0.160 2 47476425 missense variant G/A snv 3.2E-05 7.0E-06 1
rs193922373 1.000 0.160 2 47408493 missense variant G/A snv 2.4E-05 1
rs63750027 1.000 0.160 2 47480753 missense variant A/G snv 2.4E-05 4.2E-05 1
rs63750875 0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 1
rs63749841 1.000 0.160 2 47478498 missense variant A/G snv 1.2E-05 7.0E-06 1
rs267607982 1.000 0.160 2 47475198 stop gained C/G;T snv 1.2E-05 1
rs63750797 1.000 0.160 2 47480795 missense variant A/C;G snv 1.2E-05; 4.0E-06 1
rs63749936 1.000 0.160 2 47412414 missense variant A/C;G;T snv 4.0E-06; 8.0E-06 1