Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35320474 1.000 0.080 22 24441941 3 prime UTR variant -/T delins 2
rs2709370 0.851 0.120 2 207517878 intron variant A/C snv 0.17 4
rs1042606 1.000 0.080 10 110510917 3 prime UTR variant A/C snv 0.64 1
rs1245560 1.000 0.080 10 72077662 intron variant A/C snv 0.51 1
rs1457319153 1.000 0.080 3 49531991 missense variant A/C snv 4.0E-06 1
rs3786285 0.925 0.120 18 12008848 intron variant A/C;G snv 2
rs556493 1.000 0.080 6 147228161 intron variant A/C;G;T snv 1
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs956572 0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs1390938 0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs187269 0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs61749465 0.851 0.120 8 6414832 missense variant A/G snv 2.1E-03 1.9E-03 5
rs6746896 0.851 0.120 2 96745212 intergenic variant A/G snv 0.26 4
rs6785 0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 4
rs175174 0.882 0.120 22 20140031 non coding transcript exon variant A/G snv 0.44 3
rs1610037 0.925 0.120 18 910634 3 prime UTR variant A/G snv 0.26 2
rs371131106
ACE
0.925 0.120 17 63485346 missense variant A/G snv 8.4E-05 1.6E-04 2
rs3974590 0.925 0.120 18 11892846 intron variant A/G snv 0.35 2
rs613993 0.925 0.120 18 12028581 non coding transcript exon variant A/G snv 0.33 2
rs1010419 1.000 0.080 15 86992870 intron variant A/G snv 0.55 1
rs1049269 1.000 0.080 10 72060243 3 prime UTR variant A/G snv 0.64 1
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223