Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28931588 0.701 0.200 3 41224606 missense variant G/A;C;T snv 17
rs866775781 0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs149680468 0.742 0.320 4 152326137 missense variant G/A;C;T snv 15
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs121913228 0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs377767347 0.742 0.520 18 51065549 missense variant G/A;C;T snv 14
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs398124146 0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs80338963 0.776 0.280 18 51065548 missense variant C/A;G;T snv 11
rs104894231 0.776 0.360 11 533467 missense variant C/G;T snv 9
rs1057519893 0.790 0.160 12 56085070 missense variant G/A;T snv 9
rs121917759 0.790 0.480 11 533466 missense variant G/A snv 8
rs121913468 0.827 0.160 17 39724008 missense variant G/A;C;T snv 7
rs749415085 0.807 0.160 3 179198937 missense variant C/A;G;T snv 7