Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397508687 0.827 0.080 7 117531040 frameshift variant -/GA ins 4.0E-06 5
rs2647087 1.000 0.040 6 32713272 upstream gene variant A/C snv 0.29 2
rs76371115 0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 6
rs111033566 0.742 0.280 7 142750600 missense variant A/C;T snv 11
rs1223231582 0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
rs1042636 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs777418530 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 10
rs111033567 0.882 0.040 7 142750582 missense variant A/G snv 3
rs397507442 0.925 0.040 7 142750579 missense variant A/G snv 2
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs57749775 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs12008279 0.882 0.080 X 106917472 intron variant A/G;T snv 3
rs886037775
LPL
0.882 0.120 8 19960948 missense variant A/T snv 7
rs62561366 1.000 0.040 9 95555669 intergenic variant A/T snv 3.9E-02 2
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs756322971 0.763 0.240 3 122284955 missense variant C/A;G snv 9
rs387906698 0.827 0.040 7 142751919 missense variant C/A;T snv 4.0E-06; 7.2E-05 8
rs5917027 1.000 0.040 X 106919404 intron variant C/A;T snv 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs118204082
LPL
0.851 0.120 8 19955863 missense variant C/G;T snv 1.5E-04 4
rs111033568 0.882 0.040 7 142751937 missense variant C/G;T snv 2.0E-05 3
rs772223589 0.925 0.120 7 117590391 missense variant C/G;T snv 4.0E-06; 1.2E-05 3
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182