Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs2854116 0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs56225452 0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs12137855 0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs738491 0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs886041065 0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
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
rs3480 0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs3829251 0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs11669576 0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 6
rs940553638 0.827 0.200 12 111783222 missense variant G/A snv 1.6E-05 7.0E-06 6
rs2143571 0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs4240624 0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
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
rs74315468 0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
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
rs772114791 1.000 0.040 1 55052343 missense variant G/A snv 8.0E-06 7.0E-06 1
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28