Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs1004467 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 5
rs10093110 1.000 0.040 8 105553186 intron variant G/A;T snv 1
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs10128951 1.000 0.040 12 124855901 intron variant G/A snv 0.47 1
rs10131519 1.000 0.040 14 99892957 intron variant T/C snv 0.29 1
rs10131894 1.000 0.040 14 74980176 regulatory region variant C/G snv 0.49 2
rs10139550 1.000 0.040 14 99679373 3 prime UTR variant C/G snv 0.39 1
rs10186133 1.000 0.040 2 113079367 downstream gene variant G/A;T snv 1
rs10221742 1.000 0.040 2 21196778 downstream gene variant G/A snv 0.32 1
rs10237377 1.000 0.040 7 140057336 intron variant G/T snv 0.48 1
rs10249651 1.000 0.040 7 117424571 intron variant T/C snv 0.40 1
rs10267593 1.000 0.040 7 1897625 intron variant G/A snv 0.25 1
rs1034246 1.000 0.040 6 43100632 intron variant G/T snv 0.19 1
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs10456100 1.000 0.040 6 39215694 intron variant C/T snv 0.20 2
rs1048990 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 1
rs10495907 1.000 0.040 2 43771587 upstream gene variant G/A snv 0.13 1
rs1050362 1.000 0.040 16 72096916 missense variant C/A;T snv 0.38; 2.4E-05 1
rs10512861 1.000 0.040 3 132539117 downstream gene variant G/A;T snv 1
rs1051338 0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 2
rs1065852 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 2