Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs1043210477 0.701 0.520 3 49358250 missense variant G/A snv 19
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs747126003 0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs885479 0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs1129055 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs34557412 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 15
rs867186 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs2234237 0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs2232618
LBP
0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12 5
rs368287711 0.851 0.120 11 117989554 missense variant C/A;T snv 2.0E-05; 2.4E-05 4
rs1475145065 0.882 0.080 14 24574706 missense variant C/G;T snv 4.0E-06; 8.0E-06 3
rs1764390 0.882 0.160 1 34794360 missense variant A/C;G;T snv 0.61 0.69 3
rs2664581
PI3
0.882 0.120 20 45175881 missense variant A/C snv 0.16 0.16 3
rs374520012
LBP
0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06 3
rs773520745 0.882 0.120 19 18075817 missense variant C/G;T snv 2.0E-05; 4.0E-06 3