Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554888939 0.683 0.640 9 137798823 missense variant G/T snv 58
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs267606959 0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 19
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs11669576 0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 6
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs940553638 0.827 0.200 12 111783222 missense variant G/A snv 1.6E-05 7.0E-06 6
rs3213445 0.851 0.120 22 50577409 missense variant T/C snv 0.12 8.9E-02 4
rs797044485 0.851 0.160 1 156134832 missense variant G/A snv 4
rs951599607 0.925 0.040 3 12434028 missense variant G/A snv 4
rs2294918 0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs74315468 0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs1420472625 0.925 0.040 19 54178800 missense variant G/C snv 2
rs2862954 0.925 0.040 10 100152307 missense variant T/C snv 0.34 0.32 2
rs1346324047
LPA
1.000 0.040 6 160640717 missense variant G/A snv 1
rs748204991 1.000 0.040 11 130196396 missense variant G/A snv 2.1E-05 7.0E-06 1