Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs113994097 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs34778348 0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs1555507479 0.807 0.160 16 56336799 missense variant C/A snv 12
rs242557 0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs398122403 0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10