Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs754536745 0.882 0.080 19 11120144 missense variant G/A;T snv 2.0E-05 5
rs769737896 0.851 0.080 19 11110759 stop gained C/A;G;T snv 4.0E-06; 4.0E-06; 8.0E-06 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
rs879254459 0.882 0.080 19 11102771 missense variant G/A snv 5
rs879254535 0.925 0.080 19 11105369 missense variant T/A;C;G 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
rs879254900 0.882 0.080 19 11113612 missense variant T/C snv 5
rs1057516127 0.925 0.080 19 11123200 stop gained G/T snv 7.0E-06 4
rs1057519669 0.925 0.080 19 11113347 missense variant A/G snv 4
rs1057519670 0.925 0.080 19 11113406 missense variant A/T snv 4
rs1057519673 0.925 0.080 19 11113705 frameshift variant C/- del 4
rs1057519677 0.925 0.080 19 11120099 missense variant T/G snv 4
rs121908024 0.925 0.080 19 11100252 stop gained C/T snv 8.0E-06 4
rs121908040 0.851 0.080 19 11106652 missense variant G/A;T snv 1.2E-05 4
rs121908042 0.925 0.080 19 11105232 missense variant G/A;C;T snv 4.0E-06 4
rs121908044 0.925 0.080 19 11105527 synonymous variant C/G;T snv 4
rs137853964 0.925 0.080 19 11129602 missense variant G/A;T snv 1.0E-03 4
rs139624145 0.925 0.080 19 11113620 missense variant G/A;C;T snv 4.0E-05 4