Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs2421947 1.000 0.040 1 171863954 intron variant C/G;T snv 2
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs45539432 0.851 0.040 1 20649109 stop gained C/T snv 4.0E-05 3.5E-05 5
rs71653619 1.000 0.040 1 7970934 missense variant G/A snv 7.9E-03 7.0E-03 4
rs74315356 0.925 0.040 1 20649054 stop gained G/A snv 4.0E-06 1.4E-05 3
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs774005786 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 8
rs112176450 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 7
rs387907571 0.827 0.080 3 132477995 missense variant A/G snv 4.2E-06 3.5E-05 6
rs762472005 0.851 0.040 3 45722873 missense variant G/A snv 1.2E-05 7.0E-06 5
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs201106962 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs542171324 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs368134308 0.882 0.040 6 162443356 missense variant C/A;G;T snv 3.2E-05; 2.6E-04 4
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs121917763
TH
0.925 0.040 11 2167896 missense variant A/G snv 1.2E-05 7.0E-06 5
rs111501952 1.000 0.040 12 40310461 missense variant G/A snv 4.4E-05 7.7E-05 2
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs12817488 1.000 0.040 12 122811747 intron variant G/A snv 0.39 3