Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs768563000 0.925 0.080 19 11106588 stop gained G/A;T snv 2.8E-05 4
rs112029328 0.882 0.080 19 11102787 splice donor variant G/A;C;T snv 2.8E-05; 4.0E-06; 4.0E-06; 4.0E-06 5
rs121908039 0.882 0.080 19 11105457 missense variant G/A;C snv 5
rs144614838 0.882 0.080 19 11113608 missense variant G/A;T snv 2.8E-05 2.8E-05 5
rs201573863 0.882 0.080 19 11120478 missense variant C/T snv 2.0E-05 9.8E-05 5
rs376459828 0.882 0.080 19 11105496 missense variant G/A;T snv 4.0E-06 5
rs730882096 0.882 0.080 19 11110738 missense variant G/A;T snv 2.8E-05 5
rs730882109 0.882 0.080 19 11116900 missense variant C/G;T snv 4.0E-06; 1.1E-04 5
rs746118995 0.882 0.080 19 11120143 missense variant C/T snv 1.2E-05 2.8E-05 5
rs771019366 0.882 0.080 19 11102742 missense variant A/C;G snv 5
rs793888517 0.882 0.080 19 11102788 splice donor variant T/A;C snv 5
rs875989909 0.882 0.080 19 11107486 missense variant C/G snv 5
rs875989929 0.882 0.080 19 11116888 missense variant G/A;T snv 5
rs879254667 0.882 0.080 19 11106631 missense variant A/C snv 5
rs879254770 0.882 0.080 19 11110765 splice donor variant CGAAGGTG/- delins 5
rs879254867 0.882 0.080 19 11113420 stop gained G/A;C;T snv 5
rs121908025 0.851 0.080 19 11102732 missense variant T/C;G snv 2.8E-05 7.0E-06 6
rs121908026 0.851 0.160 19 11105436 missense variant C/T snv 1.6E-05 3.5E-05 6
rs121908028 0.851 0.080 19 11105587 missense variant C/A;G;T snv 8.1E-06; 8.1E-05 6
rs121908030 0.851 0.080 19 11107484 missense variant G/A;C;T snv 4.0E-06 6
rs121908031 0.851 0.160 19 11120425 stop gained C/A;G snv 8.0E-06 6
rs137943601 0.851 0.120 19 11113313 missense variant G/A;C snv 8.0E-06 6
rs139617694 0.851 0.080 19 11113534 splice acceptor variant G/A;C snv 6
rs144172724 0.851 0.080 19 11102774 stop gained G/A;T snv 1.6E-05 6
rs267607213 0.851 0.160 19 11100286 stop gained G/A;T snv 6