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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1799990 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs398122403 0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 6
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6