Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs2072115
RAPGEF3
0.882 0.080 12 47751585 intron variant A/C;G snv 5
rs3096140
GDNF ; GDNF-AS1
0.882 0.080 5 37832731 intron variant G/A snv 0.69 5
rs7209436
LINC02210-CRHR1 ; CRHR1
0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs2478813
PLXNA2
0.882 0.080 1 208073865 intron variant A/G snv 0.85 4
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs3761422
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
1.000 0.040 22 24430704 intron variant T/C snv 0.62 4
rs4752856
MTCH2
1.000 0.040 11 47626490 intron variant G/A snv 0.28 4
rs4822492
ADORA2A-AS1
1.000 0.040 22 24447626 intron variant C/G snv 0.47 4
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs10112596
GATA4
0.925 0.120 8 11722293 intron variant A/G snv 0.83 3
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs1426371
LOC105369965 ; WSCD2
1.000 0.040 12 108236003 intron variant G/A snv 0.20 3
rs17536211
GABRG1
1.000 0.040 4 46085716 intron variant A/C snv 0.14 3
rs2111902
DAO
0.925 0.080 12 108884971 intron variant T/A;G snv 0.40 3
rs2910931
MIR579 ; ZFR
0.925 0.080 5 32394809 intron variant T/A snv 0.63 3
rs353547
TWF2
0.925 0.080 3 52234850 intron variant T/C snv 0.64 3
rs3741775
DAO
0.925 0.080 12 108889827 intron variant A/C;G snv 3
rs3812047
GDNF-AS1 ; GDNF
1.000 0.040 5 37835296 intron variant C/G;T snv 3
rs4623951
DAO
0.925 0.080 12 108878275 intron variant C/G;T snv 3
rs7528604
PDE4B
0.925 0.040 1 65941669 intron variant G/A snv 0.42 3
rs112146896
EFHD2
1.000 0.040 1 15418527 intron variant A/C;G;T snv 2