Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs7157599 0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 6
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs2344484 0.925 0.040 5 135540941 upstream gene variant A/G snv 0.47 3
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs6584400 0.851 0.120 10 81896770 intron variant G/A snv 0.22 6
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1018381 0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs8074995 0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs10748842 0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs1800557
APP
0.925 0.040 21 25891795 missense variant G/A snv 4.0E-05 4.2E-05 3
rs1315695444 1.000 0.040 1 169611580 missense variant C/G snv 4.0E-06 1.4E-05 2
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237