Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs267606661 0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs573658040 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs769455 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs879254693 0.807 0.160 19 11107424 missense variant T/A;C;G snv 7
rs121918393 0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs121918394 0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5
rs267606664 0.851 0.120 19 44908730 missense variant G/A;C snv 1.6E-04; 6.3E-06 5
rs199768005 0.882 0.160 19 44909057 missense variant T/A snv 4.5E-04 4.9E-04 4
rs387906567 0.882 0.200 19 44908774 missense variant C/G;T snv 6.3E-06 4
rs121918397 0.882 0.200 19 44908784 missense variant G/A;C snv 6.5E-06 3
rs879254728 0.882 0.080 19 11107511 missense variant T/C;G snv 3
rs1466963971 0.925 0.120 19 44908640 missense variant T/G snv 4.5E-06 2
rs201672011 1.000 0.080 19 44907807 missense variant G/A snv 1.2E-04 4.8E-04 2
rs121912502 0.925 0.080 15 58548387 missense variant C/T snv 1.0E-03 7.5E-04 2
rs11542037 1.000 0.080 19 44908657 missense variant C/A;T snv 5.2E-06 1
rs121918396 1.000 0.080 19 44908979 stop gained G/A snv 1.6E-05 3.5E-05 1
rs397514253 1.000 0.080 19 44908531 splice acceptor variant A/G snv 1
rs760473480 1.000 0.080 11 35189846 missense variant C/T snv 1.2E-05 1
rs757292254 1.000 0.080 19 11105453 missense variant C/T snv 4.0E-06 1