Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 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
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
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
rs8192789
CYP2A13
1.000 0.080 19 41091846 missense variant C/A;T snv 4.0E-06; 3.1E-02 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
rs2242449
DLG4
1.000 0.080 17 7192188 non coding transcript exon variant C/A;G;T snv 2
rs2399496
DRD3
0.925 0.080 3 114127166 downstream gene variant T/A snv 0.45 2
rs3813567
CHRNB4
1.000 0.080 15 78642209 intron variant G/A snv 0.77 2
rs4425326
NPY2R
0.925 0.080 4 155186084 intron variant C/T snv 0.47 2
rs4648318
DRD2
1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs4887074
LOC112268142 ; CHRNB4
1.000 0.080 15 78659768 intron variant G/C snv 0.56 2
rs4938056
HTR3B
0.925 0.080 11 113915817 intron variant C/T snv 0.51 2
rs4952
CHRNB3
0.925 0.080 8 42731922 synonymous variant C/T snv 4.3E-02 3.2E-02 2