Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
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
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs80356537 0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs63750306 0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs63750082 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13