Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs55791371 0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs5629 0.925 0.080 20 49513169 stop gained G/A;T snv 4.0E-06; 0.25 3
rs5940 0.882 0.080 2 187466977 missense variant C/T snv 1.3E-02 1.4E-02 3
rs61688134 0.882 0.080 12 21864476 missense variant C/T snv 7.4E-03 7.5E-03 3
rs7213516 0.882 0.080 17 63474189 upstream gene variant G/A snv 5.7E-02 3
rs749903604 0.882 0.080 2 21042450 missense variant G/A snv 8.0E-06 3
rs761646500 0.925 0.080 6 169237763 missense variant C/G snv 4.0E-06 3
rs779647096
PLG
0.882 0.080 6 160718313 synonymous variant T/C snv 1.2E-05 7.0E-06 3
rs7913948 1.000 0.080 10 45373441 upstream gene variant G/A snv 0.17 3
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs1144507 0.925 0.080 11 123729767 missense variant A/C;G;T snv 0.68 2
rs11748327 1.000 0.080 5 4029676 downstream gene variant C/T snv 0.21 2
rs1213545562
TH
1.000 0.080 11 2166984 synonymous variant G/A snv 9.6E-06 2
rs12487736 1.000 0.080 3 47418189 missense variant C/T snv 0.54 0.47 2
rs12541758 0.925 0.080 8 72230147 non coding transcript exon variant C/T snv 0.34 2
rs1277204441
ACE
0.925 0.080 17 63479775 missense variant C/T snv 7.0E-06 2
rs1380959039 1.000 0.080 10 77086524 synonymous variant A/G snv 4.0E-06 2
rs1384915680
TH
1.000 0.080 11 2166903 synonymous variant G/A snv 4.3E-06 2
rs1395479 1.000 0.080 4 177397037 intergenic variant C/A;T snv 2
rs16880442 0.925 0.080 5 52889863 non coding transcript exon variant G/A;T snv 2
rs16964543 1.000 0.080 19 30694303 intron variant T/C snv 0.32 2
rs1722842 0.925 0.080 15 23785809 intron variant T/C snv 0.16 2
rs180803 0.925 0.080 22 24262890 intron variant G/A;T snv 2