Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41311117 0.882 0.120 3 38550362 missense variant A/C;G;T snv 3.6E-05; 2.0E-03; 1.0E-05 3
rs199473639 1.000 0.080 3 38550469 missense variant A/C;G;T snv 1.6E-05; 4.1E-06; 4.1E-06 1
rs757532106 0.763 0.120 3 38550500 stop gained G/A snv 4.5E-05 4.9E-05 9
rs41315493 0.851 0.120 3 38550521 missense variant C/A;T snv 6.6E-03; 9.7E-05 4
rs199473329 1.000 0.080 3 38550560 stop gained C/A;T snv 4.0E-06; 1.6E-05 1
rs199473637 1.000 0.080 3 38550569 missense variant C/T snv 2.8E-05 1.4E-05 1
rs137854603 1.000 0.080 3 38550602 missense variant C/T snv 6.0E-05 2.8E-05 1
rs864622270 1.000 0.080 3 38550665 missense variant C/A;T snv 4.0E-06 1
rs199473323 1.000 0.080 3 38550756 missense variant C/G snv 1
rs199473636 1.000 0.080 3 38550791 missense variant C/A;T snv 4.0E-06 1
rs199473322 0.925 0.080 3 38550823 missense variant C/G snv 2
rs199473320 0.882 0.120 3 38550878 missense variant G/C snv 6.0E-05 4.0E-04 3
rs397514449 0.925 0.120 3 38550984 protein altering variant -/CAT delins 2
rs137854615 0.851 0.120 3 38550989 missense variant A/G snv 4
rs886037903 1.000 0.080 3 38551015 frameshift variant AG/- del 1
rs137854601 0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs199473634 0.925 0.120 3 38551036 missense variant G/A snv 4.0E-05 7.7E-05 2
rs199473309 1.000 0.080 3 38551082 missense variant C/A snv 1
rs199473629 1.000 0.080 3 38551144 missense variant C/T snv 1
rs199473305 0.925 0.080 3 38551145 missense variant C/T snv 1.4E-05 2
rs199473304 1.000 0.080 3 38551154 missense variant C/T snv 1
rs193922726 1.000 0.080 3 38551188 missense variant G/A;C snv 6.0E-05 1
rs199473302 1.000 0.080 3 38551190 missense variant A/G snv 1
rs199473299 1.000 0.080 3 38551208 missense variant T/C snv 1
rs199473628 1.000 0.080 3 38551231 missense variant T/C snv 1