Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
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
rs113994099 0.827 0.240 15 89320883 missense variant T/C snv 10
rs63750590 0.790 0.120 14 73186860 missense variant A/G snv 10
rs188286943 0.776 0.160 16 46662452 missense variant C/T snv 9
rs63750522 0.827 0.120 14 73173644 missense variant G/A;C snv 8
rs63750577 0.827 0.120 14 73186881 missense variant C/T snv 8
rs34995376 0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
rs35801418 0.827 0.120 12 40321114 missense variant A/G snv 7
rs63750416 0.851 0.120 17 46010373 missense variant A/C snv 7
rs63750802 0.851 0.080 14 73219144 missense variant T/G snv 7
rs63751032 0.851 0.080 14 73219156 missense variant T/A;G snv 7
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs3135500 0.851 0.160 16 50732975 3 prime UTR variant G/A snv 0.44 5
rs63750050 0.925 0.080 14 73198106 missense variant T/G snv 5
rs2942168 0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14 4
rs63750444 0.882 0.080 14 73192745 missense variant G/A snv 4
rs886039227 0.925 0.200 2 74378123 missense variant A/C snv 4
rs12817488 1.000 0.040 12 122811747 intron variant G/A snv 0.39 3