Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs61747728 0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs74315364 0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs5174 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs627928 0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs139315125 0.851 0.080 1 7809900 missense variant A/G snv 5.6E-03 5.0E-03 7
rs6675281 0.827 0.080 1 231818355 missense variant C/T snv 0.11 0.14 7
rs74315355 0.790 0.080 1 20644639 missense variant G/A snv 7
rs267607555 0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs4884357 0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 6
rs5177 0.851 0.120 1 53246063 3 prime UTR variant G/A;C snv 6
rs45539432 0.851 0.040 1 20649109 stop gained C/T snv 4.0E-05 3.5E-05 5
rs748343847 0.827 0.080 1 20633708 missense variant G/A snv 6.9E-05 5
rs121908160 0.882 0.080 1 10258602 missense variant A/T snv 4
rs1317187144
GBA
0.851 0.120 1 155239889 missense variant T/C snv 4.0E-06 4
rs3737983 0.851 0.120 1 53250744 missense variant G/A;T snv 0.40; 2.4E-05; 1.2E-05 4
rs150812083 0.925 1 7809893 missense variant C/G snv 5.6E-03 5.0E-03 3
rs371792178 0.925 0.040 1 97699507 missense variant G/A;C snv 3.6E-05; 1.2E-05 3
rs80356740 1.000 1 11022556 missense variant A/G snv 1.7E-05 2
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22