Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs121918313 0.851 0.080 12 12164494 missense variant G/A snv 1.6E-05 4
rs12762303 0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs1298417395 0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1440763451 0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs4845617 0.882 0.080 1 154405422 5 prime UTR variant G/A;C snv 4
rs4862423 0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs755460305 0.882 0.080 3 186732650 missense variant C/A snv 4
rs755725121 0.882 0.080 1 9716029 missense variant G/A snv 2.1E-05 7.0E-06 4
rs773297988 0.882 0.080 3 138698965 missense variant T/C snv 4.0E-06 3.5E-05 4
rs774887459 0.882 0.080 22 40405776 missense variant G/A snv 4.0E-06 4
rs877087 0.882 0.080 15 33582074 intron variant T/C;G snv 4
rs1490867890 0.882 0.080 1 150579475 missense variant G/A;C snv 3
rs201989364 0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05 3
rs537765533 0.882 0.080 2 113132839 missense variant G/C snv 2.0E-05 3
rs539179964 0.882 0.080 8 104248720 missense variant C/T snv 1.6E-05 4.2E-05 3
rs6666258 0.882 0.080 1 154841792 intron variant G/C snv 0.30 3
rs74577862 0.882 0.080 3 186843903 intron variant G/A snv 1.8E-02 3
rs750805885 0.882 0.080 1 150579475 frameshift variant -/C delins 4.7E-06 3
rs7629265 0.882 0.080 3 38607330 intron variant C/T snv 2.3E-02 3
rs8070488
HGS
0.882 0.080 17 81696901 synonymous variant T/C snv 0.21 0.26 3
rs4901536 0.925 0.080 14 54733816 intron variant T/C snv 0.67 2
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16