Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
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
rs11931074 0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs2281983 0.851 0.080 10 102231624 missense variant G/A;C;T snv 0.62; 8.3E-06 4
rs2306604 0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs3764435 0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs201106962 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1801474 0.851 0.080 6 162201165 missense variant C/T snv 7.1E-02 5.3E-02 4