Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473293 0.925 0.120 3 38551373 missense variant C/G;T snv 4.0E-06 2
rs199473625 0.882 0.120 3 38551394 missense variant T/C snv 3.2E-05 7.0E-05 2
rs199473266 0.882 0.120 3 38555697 missense variant G/C snv 2.0E-05 2
rs36210423 0.882 0.120 3 38603887 missense variant G/A;C;T snv 2.1E-04; 4.9E-03 2
rs199473634 0.925 0.120 3 38551036 missense variant G/A snv 4.0E-05 7.7E-05 2
rs41261344 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 2
rs199473147 0.925 0.120 3 38597889 missense variant G/A snv 8.8E-05 4.2E-05 2
rs12720452 0.882 0.120 3 38603758 missense variant C/T snv 2.9E-04 2.9E-04 2
rs199473045 0.925 0.120 3 38633228 missense variant C/A;T snv 8.0E-06; 2.5E-04 2
rs199473097 0.763 0.120 3 38606710 missense variant G/A snv 8.0E-06 7.0E-06 2
rs41311117 0.882 0.120 3 38550362 missense variant A/C;G;T snv 3.6E-05; 2.0E-03; 1.0E-05 2
rs45609733 0.925 0.120 3 38598998 missense variant G/A snv 4.0E-05 1.9E-04 2
rs199473062 0.827 0.120 3 38622401 stop gained C/A;G;T snv 4.1E-06 2
rs199473153 0.882 0.120 3 38597737 stop gained C/A;T snv 4.0E-06 2
rs137854606 0.882 0.120 3 38604062 missense variant C/A snv 2
rs199473207 0.882 0.120 3 38566555 missense variant G/A snv 2
rs199473190 1.000 0.040 3 38579474 missense variant C/G;T snv 8.2E-06 1
rs199473627 1.000 0.040 3 38551258 missense variant A/G snv 1
rs727504495 1.000 0.080 3 38550998 missense variant C/A;T snv 4.0E-06; 2.0E-05 1
rs28937319 1.000 0.080 3 38562485 missense variant G/A snv 7.0E-06 1
rs199473260 0.925 0.120 3 38555720 missense variant T/C snv 1.6E-05 3.5E-05 1
rs199473107 1.000 0.120 3 38606078 missense variant A/T snv 1
rs199473618 1.000 0.120 3 38554498 missense variant C/A;T snv 2.4E-05; 2.8E-04 1
rs199473594 1.000 0.120 3 38576676 missense variant C/T snv 1
rs199473569 1.000 0.120 3 38606051 missense variant G/T snv 1