Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473261 1.000 0.080 3 38555718 missense variant A/T snv 1
rs199473052 1.000 0.080 3 38630425 missense variant A/G snv 1
rs199473570 1.000 0.080 3 38605974 stop gained C/A;T snv 1
rs199473240 0.925 0.080 3 38560176 missense variant C/T snv 1
rs199473230 1.000 0.080 3 38560356 missense variant G/T snv 1
rs199473178 1.000 0.080 3 38585695 missense variant A/G snv 1
rs199473101 0.925 0.080 3 38606682 missense variant C/A;T snv 8.1E-06 1
rs199473245 0.925 0.080 3 38557236 missense variant T/C snv 1
rs199473159 1.000 0.080 3 38587471 missense variant C/T snv 5.6E-05 2.1E-05 1
rs199473091 1.000 0.080 3 38608190 missense variant G/T snv 8.0E-06 1
rs199473053 1.000 0.080 3 38630422 missense variant A/C snv 1
rs185492581 1.000 0.080 3 38630327 stop gained T/A;C snv 7.0E-06 1
rs199473639 1.000 0.080 3 38550469 missense variant A/C;G;T snv 1.6E-05; 4.1E-06; 4.1E-06 1
rs199473323 1.000 0.080 3 38550756 missense variant C/G snv 1
rs199473175 1.000 0.080 3 38585749 stop gained G/A;T snv 4.0E-06 1
rs199473281 1.000 0.080 3 38551534 missense variant T/A snv 1
rs199473149 1.000 0.080 3 38597841 missense variant G/A snv 8.0E-06 1.4E-05 1
rs199473637 1.000 0.080 3 38550569 missense variant C/T snv 2.8E-05 1.4E-05 1
rs199473082 1.000 0.080 3 38609824 missense variant G/A;C snv 1
rs199473298 1.000 0.080 3 38551238 missense variant C/T snv 4.0E-06 1
rs199473251 1.000 0.080 3 38556535 missense variant A/G snv 1
rs199473176 1.000 0.080 3 38585728 missense variant A/C snv 1
rs199473134 1.000 0.080 3 38599046 missense variant G/A snv 1.2E-05 1
rs137854602 0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 1
rs199473170 1.000 0.080 3 38585804 missense variant A/G;T snv 1