Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1403934301 0.882 0.120 17 7631317 missense variant G/A snv 3
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs16933090 0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246