Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs588765
CHRNA5
0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs324650
LOC349160 ; CHRM2
0.827 0.080 7 137008914 intron variant T/A snv 0.55 5
rs3733829
EGLN2 ; RAB4B-EGLN2
0.882 0.120 19 40804666 non coding transcript exon variant A/G snv 0.28 5
rs9332377
ARVCF ; COMT
0.882 0.120 22 19968169 intron variant C/A;T snv 5
rs11636753
CHRNB4
0.882 0.120 15 78636604 intron variant G/T snv 0.35 4
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 4
rs1451240 0.925 0.080 8 42691568 intergenic variant A/G snv 0.64 4
rs3758987
HTR3B
0.925 0.080 11 113904553 upstream gene variant T/C snv 0.32 4
rs6474412 0.925 0.120 8 42695355 upstream gene variant C/T snv 0.64 4
rs2835859
KCNJ6
0.925 0.200 21 37645860 intron variant T/C snv 0.16 3
rs4375
PLA2G6
0.925 0.080 22 38143034 non coding transcript exon variant T/C snv 0.49 3
rs660652
CHRNA3 ; CHRNA5
1.000 0.080 15 78595490 3 prime UTR variant A/G;T snv 3
rs68081839
GRIA4
0.882 0.080 11 105762027 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 3
rs848353 1.000 0.080 7 108908603 upstream gene variant A/G snv 0.14 3
rs9217
ZBTB4
1.000 0.080 17 7459769 3 prime UTR variant T/A;C snv 3
rs10798059
PLA2G4A
0.925 0.080 1 186830478 intron variant G/A snv 0.40 2
rs1131339
STX17-AS1 ; NR4A3
0.925 0.080 9 99865020 3 prime UTR variant A/G snv 0.45 2
rs12718541
FIGNL1 ; DDC
0.925 0.080 7 50482446 intron variant A/G snv 0.55 2
rs1486012 0.925 0.080 3 114120575 intergenic variant A/T snv 0.53 2
rs1909884
CHRNA7
0.925 0.120 15 32147097 intron variant G/A snv 0.41 2
rs2242449
DLG4
1.000 0.080 17 7192188 non coding transcript exon variant C/A;G;T snv 2
rs2337980
CHRNA7
0.925 0.120 15 32151995 intron variant C/T snv 0.45 2
rs2399496
DRD3
0.925 0.080 3 114127166 downstream gene variant T/A snv 0.45 2