Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs459193 0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs7528419 0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs10774625 0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs2244608 0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs2681472 0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 6
rs867186 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 6
rs1004467 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 5
rs16948048 0.925 0.040 17 49363104 intron variant A/G snv 0.37 5
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 4
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 4
rs10738607 0.925 0.080 9 22088095 intron variant A/G snv 0.42 3
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs12133641 0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 3
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 3
rs1591805 1.000 0.040 6 126395918 intron variant A/G snv 0.47 3
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 3
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 3