Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs6584400
NRG3
0.851 0.120 10 81896770 intron variant G/A snv 0.22 6
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs2189814
GRM3
0.925 0.040 7 86702440 intron variant T/A;C snv 3
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 6
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23