Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473640 1.000 0.120 3 38550338 missense variant G/A snv 4.3E-05 2.1E-05 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
rs199473637 1.000 0.080 3 38550569 missense variant C/T snv 2.8E-05 1.4E-05 1
rs199473636 1.000 0.080 3 38550791 missense variant C/A;T snv 4.0E-06 1
rs199473635 1.000 3 38550896 missense variant G/A snv 1.6E-05 1.4E-05 1
rs199473634 0.925 0.120 3 38551036 missense variant G/A snv 4.0E-05 7.7E-05 2
rs199473632 1.000 0.120 3 38551072 missense variant T/C snv 1
rs199473631 0.925 0.120 3 38551085 missense variant C/T snv 1
rs199473629 1.000 0.080 3 38551144 missense variant C/T snv 1
rs199473628 1.000 0.080 3 38551231 missense variant T/C snv 1
rs199473627 1.000 0.040 3 38551258 missense variant A/G snv 1
rs199473626 1.000 0.080 3 38551357 missense variant G/T snv 1
rs199473625 0.882 0.120 3 38551394 missense variant T/C snv 3.2E-05 7.0E-05 2
rs199473624 1.000 0.080 3 38551447 missense variant C/T snv 1
rs199473623 0.882 0.120 3 38551486 missense variant C/T snv 1.2E-05 7.0E-06 1
rs199473622 1.000 0.120 3 38551546 stop gained G/A;C;T snv 1.2E-05 1
rs199473621 1.000 0.080 3 38554344 missense variant C/T snv 2.0E-05 2.1E-05 1
rs199473620 1.000 0.080 3 38554372 stop gained C/A;T snv 1
rs199473619 1.000 0.120 3 38554412 missense variant C/G snv 4.0E-06 1
rs199473618 1.000 0.120 3 38554498 missense variant C/A;T snv 2.4E-05; 2.8E-04 1
rs199473617 1.000 0.080 3 38554530 missense variant A/G;T snv 1
rs199473616 1.000 0.120 3 38555731 missense variant C/A snv 4.0E-06 1
rs199473615 0.925 0.120 3 38555742 missense variant A/G snv 1
rs199473614 1.000 0.080 3 38556491 missense variant T/A snv 1
rs199473613 1.000 0.080 3 38556532 missense variant T/C snv 1